Hyaluronidase from bovine testes, CAS No.37326-33-3

CAS: 37326-33-3 Cat. No.: H754935 Número EC: 253-464-3

GRADE & PURITY Bioactive, ActiBioPure™, Native, Endotoxin tested, High Performance, EnzymoPure™, 400-1000 IU/mg enzyme powder

Accession #

Q5E985,Q8SQG8

Endotoxin Concentration

<0.2 EU/IU

Bioactivity

400-1000 IU/mg enzyme powder

Descripción general

Hyaluronidase from bovine testes has been used for the digestion of breast tissue, heart tissue and oocytes for isolation of cells.

Suitable for use in preparation of single cell suspension for sequencing.

Hyaluronidase degrades hyaluronan and has been found to be inappropriately regulated during cancer progression.

These enzymes randomly cleave β-N-acetylhexosamine-[1→4] glycosidic bonds in hyaluronic acid, chondroitin, and chondroitin sulfates.

Specifications

Product Name

Hyaluronidase from bovine testes, CAS No.37326-33-3

Sinónimos

Hyaluronate 4-glycanohydrolase | Hyaluronoglucosaminidase | hyaluronoglucosaminidase | chondroitinase | chondroitinase I | hyaluronidase | hyaluronoglucosidase | Hyaluronate 4-glycanohydrolase | HYAL1 | HYAL2

Grado

ActiBioPure™, Bioactive, Endotoxin tested, High Performance, Native, EnzymoPure™

Especificaciones y pureza

Bioactive, ActiBioPure™, Native, endotoxin tested, High Performance, EnzymoPure™, 400-1000 IU/mg enzyme powder

Mecanismos bioquímicos y fisiológicos

Hyaluronidase degrades hyaluronan and has been found to be inappropriately regulated during cancer progression. These enzymes randomly cleave β-N-acetylhexosamine-[1→4] glycosidic bonds in hyaluronic acid, chondroitin, and chondroitin sulfates.

Bioactividad

400-1000 IU/mg enzyme powder

Concentración de endotoxinas

<0.2 EU/IU

Número de adhesión

Q5E985, Q8SQG8

CAS

37326-33-3

Número de la Comisión de Enzimas

3.2.1.35(BRENDA, IUBMB)

Tipo de molécula

Enzyme

Almacenamiento y envío

Concentración

400-1000 IU/mg enzyme powder

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Definición de unidad

One unit (IU) of hyaluronidase is defined as the amount of enzyme required to hydrolyze hyaluronic acid to produce reducing sugars equivalent to 0.5 μg of glucuronic acid per minute at 37 ℃ and pH 5.3.

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Indoles and derivatives
      • Subclass Indolyl carboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Indoles and derivatives
• Subclass: Indolyl carboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Indolyl carboxylic acids and derivatives
• Alternative Parents: Indoles Tertiary alkylarylamines Medium-chain fatty acids Heterocyclic fatty acids Amino fatty acids Benzenoids Amino acids Monocarboxylic acids and derivatives Enamines Carboxylic acids Azacyclic compounds Organic oxides Hydrocarbon derivatives Hydrobromides Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Indolyl carboxylic acid derivative - Indole - Medium-chain fatty acid - Tertiary aliphatic/aromatic amine - Amino fatty acid - Heterocyclic fatty acid - Fatty acyl - Benzenoid - Amino acid or derivatives - Amino acid - Tertiary amine - Carboxylic acid derivative - Carboxylic acid - Azacycle - Enamine - Monocarboxylic acid or derivatives - Amine - Organonitrogen compound - Organooxygen compound - Hydrobromide - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. These are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring.
• External Descriptors: Not available

Data sources

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

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