CD11a / ITGAL Mouse Monoclonal Antibody [Clone ID: 8-6.2]
CAT#: CL013R
CD11a / ITGAL mouse monoclonal antibody, clone 8-6.2, PE
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CNY 3,652.00
货期*
5周
规格
Specifications
Product Data | |
Clone Name | 8-6.2 |
Applications | FC |
Recommend Dilution | Flow Cytometry (See Protocols). |
Reactivity | Mouse |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | B6-Ly-1a Thymus, spleen and lymph node. Donor: 129/ReJ spleen Fusion Partner: P3-NS-1 Ag-4 |
Specificity | This CD11a Monoclonal Antibody identifies a cell surface glycoprotein consisting of two non-covalently associated chains with molecular weights of 180kDa (Alpha chain) (1) present on most common lymphocytes and T and B cells. |
Formulation | PBS containing 0.02% Sodium Azide as preservative and EIA grade BSA as a stabilizing protein to bring total protein concentration to 4-5 mg/ml Label: PE State: Liquid purified Ig fraction |
Concentration | lot specific |
Purification | Protein G Chromatography |
Conjugation | PE |
Storage Condition | Store the antibody undiluted at 2-8°C. DO NOT FREEZE! This product is photosensitive and should be protected from light. |
Database Link | |
Background | CD11a is a member of the integrin family of cell adhesion molecules. It is a glycoprotein expressed in combination with the CD18 beta chain. The complex is a member of the beta 2 integrin family. These molecules function in cell adhesion and specifically bind to CD54, ICAM2, ICAM3. CD11a is expressed on thymocytes, T and B lymphocytes, granulocytes, monocytes, and macrophages. |
Synonyms | Integrin alpha-L, LFA1, LFA-1 |
Note | Protocol: Flow Cytometry Analysis: Method: 1. Prepare a cell suspension in media A. For cell preparations, deplete the red blood cell population with Lympholyte®-M cell separation medium. 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 1x106 cells, representing 1 test). 4. To each tube, add ~2.0 µg* of CL013R or CL013RX. 5. Vortex the tubes to ensure thorough mixing of antibody and cells. 6. Incubate the tubes for 30 minutes at 4°C. (It is recommended that the tubes are protected from light since most fluorochromes are light sensitive). 7. Wash 2 times at 4°C. 8. Resuspend the cell pellet in 50 µl ice cold media B. 9. 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). Results: Tissue Distribution by Flow Cytometry Analysis: Mouse Strain: CBA/J Cell Concentration : 1x10e6 cells per test Antibody Concentration Used: 2.0 µg/106 cells Isotypic Control: PE Mouse IgG2a Cell Source Percentage of cells stained above control: Thymus: 98.3% Lymph Node: 99.6 Strain Distibution: Cell Concentration: 1x10e6 cells per test Antibody Concentration Used: 1.0 µg/10e6 cells Strains Tested: /6, BALB/c, AKR, CBA/J, C3H/HE Positive: C57BL/6, CBA/J, C3H/He Negative: BALB/c, AKR |
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