MHC Class II I-Ap antibody
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- Target
- MHC Class II I-Ap
- Reactivity
- Mouse
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Host
- Mouse
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Clonality
- Monoclonal
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Conjugate
- Un-conjugated
- Application
- Flow Cytometry (FACS), Cytotoxicity Test (CyTox)
- Purification
- Ig Fraction
- Immunogen
- Recipient: BALB/c Donor: B10.P Fusion Partner: Spleen from immunized recipient fused with myeloma SP2/0
- Clone
- 7-16-17
- Isotype
- IgG2a
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- Application Notes
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Cytotoxicity analysis.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. - Protocol
- RECOMMENDED METHOD FOR DEPLETING A CELL POPULATION OF I-A ANTIGEN BEARINGCELLS: 1. Prepare a cell suspension from the appropriate tissue in Cytotoxicity Medium®1 orequivalent. Remove red cells and dead cells (where necessary) by purification of viablelymphocytes on Lympholyte-M®2 density cell separation medium. After washing, adjustthe cell concentration to 1 x 10e7 cells per ml in Cytotoxicity Medium. 2. Add the antibody to a final concentration of 1: 40 and mix. Alternatively, pellet the cellsand resuspend in antibody diluted 1: 40 in Cytotoxicity Medium. 3. Incubate for 60 minutes at 4°C.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Reconstitution
- Restore with 1.0 mL of distilled water.
- Buffer
- PBS
- Precaution of Use
- Use of sodium azide as a preservative will substantially inhibit the enUse of sodium azide as a preservative will substantially inhibit the enzyme activity of horseradish peroxidase.
- Handling Advice
- Avoid repeated freezing and thawing. Should this product contain a precipitate we recommend microcentrifugation before use.
- Storage
- -20 °C
- Storage Comment
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Target
- MHC Class II I-Ap
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