Name: Ethylenediaminetetraacetic acid(EDTA) - for cell culture, ≥99% , CAS No.60-00-4
Brand: Aladdin Scientific
SKU: E112489
Availability: InStock

Vue d’ensemble Spécifications Noms et identifiants Documentation Données avancées Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

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Pourquoi cette qualité

for cell culture, ≥99% pour la culture cellulaire pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Room temperature Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 1010 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Application：

Ethylenediaminetetraacetic acid has been used:as a component of peptide dilution buffer for intracellular BH3 (Bcl-2 homology (BH) domain) profiling and validation；as a medium component in the hepatic stellate cell (HSCs) culture；as a component of homogenization buffer for protein extraction from eye tissues；for stopping benzonase reaction in lysis buffer.

Spécifications

Synonymes

EDTA | Edetic acid | Edathamil | (Ethylenedinitrilo)tetraacetic acid

Spécifications et pureté

for cell culture, ≥99%

Mécanismes biochimiques et physiologiques

Biochem/physiol Actions：Ethylenediaminetetraacetic acid (EDTA) is an anticoagulant, majorly used in preventing clotting of blood samples.EDTA may trigger aggregation of platelets resulting in pseudothrombocytopenia.EDTA along with tetracycline imparts ser

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

pour la culture cellulaire

Pureté

≥99%

Noms et identifiants

Pubchem Sid

508811765

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811765

Sourires canoniques

C(CN(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O

IUPAC Name

2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid

InChIKey

KCXVZYZYPLLWCC-UHFFFAOYSA-N

INCHI

1S/C10H16N2O8/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20)

Isomères SMILES

C(CN(CC(=O)O)CC(=O)O)N(CC(=O)O)CC(=O)O

Poids moléculaire

292.24

Reaxy-Rn

1716295

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1716295&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Carboxylic acids and derivatives
    - Subclass Tetracarboxylic acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Carboxylic acids and derivatives
Subclass	Tetracarboxylic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Tetracarboxylic acids and derivatives
Alternative Parents	Alpha amino acids Trialkylamines Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Tetracarboxylic acid or derivatives - Alpha-amino acid - Alpha-amino acid or derivatives - Amino acid or derivatives - Tertiary amine - Tertiary aliphatic amine - Amino acid - Carboxylic acid - Organopnictogen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Amine - Organic oxide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.
External Descriptors	ethylenediamine derivative - polyamino carboxylic acid - tetracarboxylic acid
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

F2 Tclin Thrombin (11687 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PGR Tclin Progesterone receptor (8562 Activities)

Discover Target: PGR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

Discover Target: CHRM2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

Discover Target: ADRB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

Discover Target: HTR1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOA Tclin Monoamine oxidase A (11911 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHE Tclin Acetylcholinesterase (18204 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

Discover Target: PTGS1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HRH2 Tclin Histamine H2 receptor (5428 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

Discover Target: HTR2A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

Discover Target: HTR2C

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)

Discover Target: AVPR2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A4 Tclin Serotonin transporter (12625 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

Discover Target: ADRA1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HRH1 Tclin Histamine H1 receptor (7573 Activities)

Discover Target: HRH1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRM1 Tclin Mu opioid receptor (19785 Activities)

Discover Target: OPRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD3 Tclin Dopamine D3 receptor (14368 Activities)

Discover Target: DRD3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

Discover Target: AVPR1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRD1 Tclin Delta opioid receptor (15096 Activities)

Discover Target: OPRD1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRK1 Tclin Kappa opioid receptor (16155 Activities)

Discover Target: OPRK1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)

Discover Target: HTR3A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A3 Tclin Dopamine transporter (10535 Activities)

Discover Target: SLC6A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)

Discover Target: GRIN1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KCNH2 Tclin HERG (29587 Activities)

Discover Target: KCNH2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)

Discover Target: CACNA1C

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

Discover Target: PDE3A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)

Discover Target: SLC29A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)

Discover Target: ADRA2B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)

Discover Target: ADRA2C

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)

Discover Target: CHRM3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)

Discover Target: HTR2B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)

Discover Target: TBXA2R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADORA2A Tclin Adenosine A2a receptor (16305 Activities)

Discover Target: ADORA2A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PDE4A Tclin Phosphodiesterase 4A (1943 Activities)

Discover Target: PDE4A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

Discover Target: ADORA3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

blaZ Beta-lactamase (285 Activities)

Discover Target: blaZ

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mc4r Melanocortin receptor 4 (1205 Activities)

Discover Target: Mc4r

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mmp13 Matrix metalloproteinase 13 (19 Activities)

Discover Target: Mmp13

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Npy1r Neuropeptide Y receptor type 1 (8 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cckar Cholecystokinin A receptor (90 Activities)

Discover Target: Cckar

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pde4d Phosphodiesterase 4D (4 Activities)

Discover Target: Pde4d

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Hdac6 Histone deacetylase 6 (222 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Klebsiella pneumoniae (43867 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Staphylococcus aureus (210822 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Staphylococcus epidermidis (22802 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Escherichia coli (133304 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Enterococcus faecalis (29875 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mycolicibacterium smegmatis (8003 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Candida parapsilosis (8521 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mus musculus (284745 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Carbapenem-hydrolizing beta-lactamase SFC-1 (31 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

imiA IMI-1 (34 Activities)

Discover Target: imiA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

bla Carbepenem-hydrolyzing beta-lactamase KPC (120 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pseudoalteromonas (41 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Ileum (29 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

blaVIM-13 Class B carbapenemase VIM-13 (33 Activities)

Discover Target: blaVIM-13

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

blaVIM Beta-lactamase VIM-1 (33 Activities)

Discover Target: blaVIM

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

bla2 Beta-lactamase II (21 Activities)

Discover Target: bla2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cell membrane (1233 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

cAMP-specific 3',5'-cyclic phosphodiesterase 4B (18 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

bla(NDM-4) Metallo-beta-lactamase NDM-4 (34 Activities)

Discover Target: bla(NDM-4)

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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33 results found

Lot Number	Certificate Type	Date	Article
G2531371	Certificate of Analysis	Jul 31, 2025	E112489
G2531264	Certificate of Analysis	Jul 10, 2025	E112489
E2625035	Certificate of Analysis	Jul 10, 2025	E112489
G2531372	Certificate of Analysis	Jul 10, 2025	E112489
G2610075	Certificate of Analysis	Jul 10, 2025	E112489
H2507857	Certificate of Analysis	Jul 10, 2025	E112489
K2521029	Certificate of Analysis	Apr 08, 2025	E112489
D2527230	Certificate of Analysis	Apr 08, 2025	E112489
D2527229	Certificate of Analysis	Apr 08, 2025	E112489
D2527228	Certificate of Analysis	Apr 08, 2025	E112489
C2617075	Certificate of Analysis	Apr 08, 2025	E112489
K2518219	Certificate of Analysis	Apr 08, 2025	E112489
C2521282	Certificate of Analysis	Dec 21, 2024	E112489
A25031014	Certificate of Analysis	Dec 21, 2024	E112489
A25031013	Certificate of Analysis	Dec 21, 2024	E112489
A25031005	Certificate of Analysis	Dec 21, 2024	E112489
C2525124	Certificate of Analysis	Oct 08, 2024	E112489
J2415767	Certificate of Analysis	Oct 08, 2024	E112489
G2417775	Certificate of Analysis	Jun 28, 2024	E112489
G2417777	Certificate of Analysis	Jun 28, 2024	E112489
G2417778	Certificate of Analysis	Jun 28, 2024	E112489
E2428618	Certificate of Analysis	May 17, 2024	E112489
G2405064	Certificate of Analysis	May 17, 2024	E112489
E2428593	Certificate of Analysis	May 17, 2024	E112489
E2428592	Certificate of Analysis	May 17, 2024	E112489
H2211299	Certificate of Analysis	Jul 21, 2022	E112489
H2211300	Certificate of Analysis	Jul 21, 2022	E112489
H2211301	Certificate of Analysis	Jul 21, 2022	E112489
C2418051	Certificate of Analysis	Jul 21, 2022	E112489
B2303870	Certificate of Analysis	Jul 21, 2022	E112489
A2218374	Certificate of Analysis	Dec 15, 2021	E112489
A2218376	Certificate of Analysis	Dec 15, 2021	E112489
A2218375	Certificate of Analysis	Dec 15, 2021	E112489

Propriétés chimiques et physiques

Solubilité	The solubility in water at 25 ℃ is 0.5g/L. Insoluble in cold water, alcohols, and general organic solvents. Soluble in sodium hydroxide, sodium carbonate, and ammonia solutions.
Point de fusion (°C)	220°C
Poids moléculaire	292.240 g/mol
XLogP3	-5.900
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	10
Rotatable Bond Count	11
Exact Mass	292.091 Da
Monoisotopic Mass	292.091 Da
Topological Polar Surface Area	156.000 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	315.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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DNA ligases

A Comprehensive Overview of Zinc Ion Fluorescent Probes: From TSQ / Zinquin to ZnAF / Zinpyr-1 – Mechanistic Comparison and Aladdin Selection Guide

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Fluorescent probes Zn Zinc ion fluorescent probe

Protease & Phosphatase Inhibitor Cocktails: Research Applications and Principles

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Cell lysis Protein extraction Tissue homogenate

Tyrosinase: a key regulatory enzyme in melanin synthesis and its biological and applied significance

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Oxidizing agent Molecular oxygen

Molecular Mechanisms and Biomedical Applications of Heparinase

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Lytic enzyme

Molecular Mechanisms and Multidomain Applications of Inorganic Pyrophosphatase

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Inorganic pyrophosphatase

His-Tag Protein Purification: Common Troubleshooting Questions and Practical Solutions

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His-tag protein purification

Nucleic Acid and Nuclease Decontamination in Biopharmaceutical Manufacturing and Molecular Testing Workflows

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Nucleic acid Nuclease Biopharmaceutical

Technical Analysis and Application Guide for RNase Inhibitors

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RNase RNase Inhibitors

Laccase: Technical Characteristics, Optimization Strategies, and Industrial Application Progress

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laccase multicopper oxidase T1/T2/T3 copper centers laccase-mediator system immobilization protein engineering industrial decolorization biobleaching

Endoproteinase Lys-C: Mechanism, Applications, and Method-Control Considerations for Lysine-Specific Digestion

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Peptide Mapping Serine protease Lys-C Endoproteinase Lys-C Lysine-specific cleavage Denaturing digestion LC–MS Sequence coverage Missed cleavage rate Critical peptide monitoring Method validation

Protein Tags Demystified: Classification, Properties, and Suitable Experimental Applications

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protein tags affinity tags epitope tags fluorescent tags affinity purification

Proteinase K: Frequently Asked Questions

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Proteinase K

How Organic Acids “Stabilize a System”: Selection Logic via the pH Window, Salt Forms, and Metal-Ion Management (with a navigation guide to Tables A–E)

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Pharmaceuticals Organic Acids

Phycocyanin: A Review of Sources, Structural Features, Production Processes, Applications, and Claimed Benefits

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stability Fluorescent labeling phycocyanin C-phycocyanin R-phycocyanin phycobiliproteins natural edible colorant fluorescent phycocyanin

Amino Acid Oxidases: Oxygen-Dependent Oxidative Deamination Systems and Their Analytical and Applied Uses

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Biosensing FAD FMN Amino acid oxidase L-amino acid oxidase D-amino acid oxidase Oxidative deamination Hydrogen peroxide Chiral analysis Oxygen limitation

RNA Extraction Technologies: Method Systems, Operational Workflows, and Key Quality-Control Considerations

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RNA extraction RNase Magnetic beads Column-based method organic extraction DNase treatment A260/280 A260/230 RIN

Agarose Precast Gels: Composition, Advantages, and Application Workflows for Standardized Nucleic Acid Electrophoresis Matrices

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DNA Nucleic acid electrophoresis agarose precast gels RNA resolution pore size buffer system wells lot-to-lot consistency band sharpness gel extraction standardization high-throughput

Procyanidins: Structural Features and Key Points for Research and Application

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Epicatechin procyanidins OPC PPC catechin

Phytase: Enzymological Properties, Mechanism of Action, and Applications in Feed and Food

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submerged fermentation Phytase Phosphomonoesterase Phytate Myo-Inositol Hexakisphosphate Available Phosphorus Monogastric Animals Pelleting Stability Solid-State Fermentation

Chlorophyll: Structural Features, Physicochemical Properties, and Key Points for Research and Industrial Applications

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stability HPLC Fluorescence Magnesium chlorophyll chlorophyll a chlorophyll b porphyrin ring phytol pheophytin Cu/Zn complexes

Ferulic Acid: Structural Features, Preparation Routes, and Key Points for Research Applications

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ferulic acid 3-methoxy-4-hydroxycinnamic acid

Flavones: Structural Features, Physicochemical Properties, and Key Points for Research and Applications

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HPLC Antioxidation flavone C6–C3–C6 flavone glycosides O-glycosides C-glycosides C5-hydroxylation 5-deoxy flavones TLR/NF-κB heterologous biosynthesis

dsDNase-Mediated Hydrolysis of Double-Stranded DNA: Enzymatic Characteristics, Methodological Strategies, and Bioanalytical Applications

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Biopharmaceuticals double-stranded deoxyribonuclease dsDNase dsDNA hydrolysis nucleic-acid removal sample pretreatment contamination control

Alginate : An Overview of Extraction and Purification Processes, Quality Identification, and Multidomain Applications

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Quality control Alginate Sodium alginate Calcium alginate Brown algae M/G ratio Ionic crosslinking Identification

Functional Properties, Application Scenarios, and Manufacturing Processes of Maltotetraose (G4): A Review

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G4 Maltotetraose Maltooligosaccharide α-1,4-glycosidic bond Low sweetness High viscosity Anti-crystallization Acid and heat stability

Review of Chymotrypsin: Enzymological Properties, Catalytic Mechanism, and Research Applications

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Peptide Mapping Serine protease substrate specificity limited proteolysis catalytic triad Chymotrypsin Alpha-Chymotrypsin Oxyanion Hole Acyl-Enzyme Intermediate Methodological Quality Control

Clostridial Proteases: Classification, Molecular Mechanisms, and Research Applications

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clostridial proteases

Review of the Principles, Methods, and Application Considerations for Superoxide Dismutase Activity Determination

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Oxidative Stress activity assay Methodological standardization SOD Superoxide Dismutase NBT assay WST assay Pyrogallol Autoxidation Assay Xanthine Oxidase Assay Antioxidant Evaluation

Tissue Dissociation for Single-Cell Preparation: Sample Handling and Quality Control Strategies

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cell viability single-cell preparation tissue processing sample quality control enzymatic digestion doublets declumping dead cell removal single-cell transcriptomics flow sorting

Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression

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Peptide synthesis Liquid-phase peptide synthesis

Perovskite Oxides for Energy and Environmental Catalysis: How Oxygen Vacancies, B-Site Metals, and the Metal–Oxygen Bond Network Regulate Reaction Performance

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perovskite perovskite oxides oxide

What Are Polyamines? Structural Features, Classification and Representative Compounds, Applications, and Synthetic Strategies

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Organic chemistry Medicinal Chemistry Polyamine Multiple amine nitrogen atoms Nitrogen-containing organic compounds

The Role, Selection, and Validation of Chelating Agents in Daily Chemical Formulations

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Chelating Agents

From Structure to Rheology: How Carbomer Forms Gel Structures and Enables Thickening, Suspension, and Auxiliary Emulsion Stabilization

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Carbomer

From Structure to Selection: Mechanisms and Application Assessment of Low-Foam Oil and Wax Removal with Fatty Acid Methyl Ester Ethoxylates (FMEE)

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FMEE MEE

Sodium Metasilicate in Cleaning Applications: Hydration-Form Differences, Mechanisms of Action, and Selection Logic

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Na₂SiO₃ Sodium Metasilicate

Bone Tissue Decalcification Protocol: Rapid and Slow Methods

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Bone tissue decalcification

GITC——Key Reagent for Nucleic Acid Extraction and Sample Protection

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RNA extraction DNA extraction GITC Nucleic Acid Extraction Sample Protection Virus Inactivation Protein Denaturant Molecular Diagnosis

Aladdin® Plant Research Related Products

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Plant tissue culture Genetic transformation Botany Phytohormones Protoplasts Infection

Bacterial Cell Wall Degradation Technology

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SDS Proteinase K Cell lysis EDTA Protoplasts Lysozyme Gram-negative bacteria Gram-positive bacteria Bacterial cell wall Peptidoglycan Lysostaphin

Phase-Partitioning Principles, System Differences, and Application Selection in Phenol-Based DNA and RNA Extraction

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RNA extraction DNA extraction Quality control phenol-based extraction phenol-chloroform isoamyl alcohol acidic phenol guanidinium thiocyanate liquid-liquid partitioning nucleic acid purification

What Determines Collagen Function: From Triple-Helix Formation to Hierarchical Assembly, Crosslink Maturation, and Dynamic Remodeling

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Collagen

The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis

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peptide palmitoyl chain

Differences Between Animal-Derived Collagen and Recombinant Collagen in Skincare: Sequence and Structure, Safety, Skin Effects, and Evidence Evaluation

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Animal-Derived Collagen Recombinant Human Collagen Recombinant Humanized Collagen Triple Helix Immunogenicity Skin Repair Transepidermal Water Loss

Regulatory Mechanisms of 5mC DNA Methylation

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Epigenetics DNA methylation 5mC DNMT TET 5hmC UHRF1 TDG

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Acide éthylènediamine-tétraacétique - Ultra pur, anhydre, ≥99,5%(T) , CAS No.60-00-4

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