MHC Class II I-Ab Mouse Monoclonal Antibody [Clone ID: 25-5-16S]
CAT#: SM080B
MHC Class II I-Ab mouse monoclonal antibody, clone 25-5-16S, Biotin
Conjugation: Unconjugated
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CNY 4,466.00
货期*
5周
规格
Specifications
Product Data | |
Clone Name | 25-5-16S |
Applications | FC |
Recommend Dilution | Flow Cytometry (see protocol below). |
Reactivity | Mouse |
Host | Mouse |
Clonality | Monoclonal |
Specificity | This antibody specifically reacts with the I-Ab encoded MHC Class II alloantigen expressed on mouse strains BXSB/Mp, C57BL/ 6, C57BL/10, LP/J, and 129. Tissue Distribution by Flow Cytometry Analysis: Representative Histogram Mouse Strain: C57BL/6 Cell Concentration : 1x10e6 cells per test Antibody Concentration Used: 0.5 µg/10e6 cells Isotypic Control: Biotin Mouse IgM. |
Formulation | PBS containing 0.09% Sodium Azide and EIA grade BSA as a stabilizing protein to bring total protein concentration to 4-5 mg/ml. Label: Biotin State: Liquid purified Ig fraction |
Concentration | lot specific |
Conjugation | Biotin |
Storage Condition | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Database Link | |
Synonyms | H2-Eb1, H-2 class II histocompatibility antigen I-A beta chain |
Note | Protocol: FLOW CYTOMETRY ANALYSIS: Method: 1. Prepare a cell suspension in media A. For cell preparations, deplete the red blood cell population. 2. Wash 2 times. 3. Resuspend the cells to a concentration of 2x10e7 cells/ml in media A. Add 50 µl of this suspension to each tube (each tube will then contain 1 x 10e6 cells, representing 1 test). 4. To each tube, add 0.5-1.0 µg of antibody per 10e6 cells. 5. Vortex the tubes to ensure thorough mixing of antibody and cells. 6. Incubate the tubes for 30 minutes at 4°C. 7. Wash 2 times at 4°C. 8. Add 100 µl of secondary antibody Streptavidin-FITC at a 1:500 dilution. 9. Incubate tubes at 4°C for 30 - 60 minutes (It is recommended that tubes are protected from light since most fluorochromes are light sensitive). 10. Wash 2 times at 4°C. 11. Resuspend the cell pellet in 50 µl ice cold media B. 12. Transfer to suitable tubes for flow cytometric analysis containing 15 µl of propidium iodide at 0.5 mg/ml in PBS. This stains dead cells by intercalating in DNA. Media: A. Phosphate buffered saline (pH 7.2) + 5% normal serum of host species + sodium azide (100 µl of 2M sodium azide in 100 mls). B. Phosphate buffered saline (pH 7.2) + 0.5% Bovine serum albumin + sodium azide (100 µl of 2M sodium azide in 100 mls). |
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