Aladdin's UltraBio™ Anti-HA Agarose is produced by high-quality HA antibodies to 4% agarose gel. The HA antibody is a high-affinity mouse monoclonal antibody that recognizes the HA epitope tag (YPYDVPDYA) derived from the human influenza hemagglutinin (HA) protein. The HA tag can be located at the N-terminus, C-terminus, or an internal position of the protein, such as N-terminal HA fusion protein (HA-Protein), C-terminal HA fusion protein (Protein-HA), and Met-modified N-terminal HA fusion protein (Met-HA-Protein).This agarose can specifically bind HA fusion proteins in lysates, serum, ascites, or other samples from animals, plants, or microorganisms. This product is mainly used for immunoprecipitation (IP), co-immunoprecipitation (Co-IP), or purification of HA-tagged proteins or their protein complexes.
Aladdin UltraBio™ Anti-HA Agarose is stored in PBS containing 0.02% ProClin 300, with a settled gel to storage solution ratio of 1:1(This product is a 50% gel suspension, containing 0.5 ml of settled agarose per milliliter. Our product specifications are based on total volume. Product information is detailed in the table below:
Parameter | Value/Description | Matrix | 4% Agarose Microspheres | Ligand | HA tag Mouse mAb | Isotype | Mouse IgG2b | Particle Size Range | 45~165 μm | Antibody concentration | Approximately 3 mg HA tag Mouse mAb/mL Settled Agarose | Maximum Pressure | 0.3 MPa，3 bar | Storage Conditions | PBS contains 0.02% ProClin 300, 2-8℃ | Shelf Life | 1 year |
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Instruction for use
1. Sample Preparation
1.1 Ensure the sample solution has appropriate ionic strength and pH before loading. Dilute the sample or cell culture supernatant with equilibration buffer, or dialyze the sample against equilibration buffer.
1.2 Clarify the sample by centrifugation or filtration through a 0.22 μm or 0.45 μm membrane to reduce impurities, improve purification efficiency, and prevent column clogging.
1.3 Preparation of protein sample. Lysis cells or tissues with appropriate lysis buffer. The following lysis buffers are recommended for preparing lysates from cells or tissues. For optimal results, Aladdin product C301898 Cell Total Protein Lysate for Western Blotting & Immunoprecipitation is the preferred choice for lysis of cell or tissue samples. Depending on the specific experimental needs, if necessary, Aladdin products P0013B RIPA Lysis Buffer (Strong), P0013C RIPA Lysis Buffer (Medium), or P0013D RIPA Lysis Buffer (Weak) may also be used for sample preparation. If using a self-prepared lysis buffer or one from another manufacturer, e nsure that the pH of the lysis buffer is between 6 and 8. when using a self-prepared lysis buffer or one produced by other companies, ensure that the pH of the lysis buffer is 6-8.
2. Buffer Preparation
It is recommended to filter water and buffers through a 0.22 μm or 0.45 μm membrane before use.
Equilibration Buffer: 0.01M PBS，pH7.4.
Wash Buffer: 0.01M PBS，0.05% Tween-20，pH7.4.
3. Immunoprecipitation (IP) Procedure
3.1 Resin Preparation: Add 40 µL of Anti-HA Agarose suspension (20 µL settled agarose) to a 1.5 mL tube. Centrifuge at 5000 × g for 1 minute. Discard the supernatant.
3.2 Add 0.5 mL of Equilibration Buffer to resuspend the agarose (Place the agarose in the same buffer system as the target protein to protect the protein.). Centrifuge at 5000 × g for 1 minute. Discard the supernatant. Repeat this wash step once.
3.3 Add 300 µL of sample lysate to the prepared agarose from step 3.2. Mix and incubate on a tube rotator at room temperature for 3 hours. Centrifuge at 5000 × g for 1 minute. Discard the supernatant.
3.4 Washing: Add 0.5 mL of Wash Buffer, resuspend the agarose, and mix gently. Centrifuge at 5000 × g for 1 minute. Discard the supernatant. Repeat this wash step three more times. Ensure the removal of non-specifically adsorbed substances.
3.5 Denaturing Elution (SDS-PAGE): Add 100 µL of 1 × Loading Buffer to the agarose. Heat at 95°C for 5 minutes. Centrifuge at 5000 × g for 1 minute, and load the supernatant directly onto an SDS-PAGE gel for analysis.
Note: The Standard loading buffer used in laboratories contains β-mercaptoethanol and DTT, which can break the disulfide bonds between the antibody heavy and light chains on the agarose. This method denatures the antibody, rendering the resin unusable for reuse.
Storage
Store at 4℃ for up to 12 months. Do not store at -20℃ or lower temperatures.
Matters needing attention
1. This product must be fully resuspended by inverting the tube several times prior to use.
2. For immunoprecipitation assays, it is recommended to include both positive and negative controls.
3. Protein samples should be purified as soon as possible after collection and should always be placed at 4℃ or on ice to minimize protein degradation or denaturation.
4. The non-specific binding capability of this product can be affected by high concentrations of DTT, mercaptoethanol, and guanidine hydrochloride, but it is applicable in Cell lysis buffer for Western and IP , RIPA Lysis Buffer , and NP-40 Lysis Buffer .
5. To effectively inhibit protein degradation, an appropriate amount of protease inhibitor cocktail can be added to the protein sample.
6. This product is for R&D only. Not for drug, household, or other uses.
7. For your safety and health, please wear a lab coat and disposable gloves during the operation.
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