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 Biotin



Need it in bulk or conjugated?
Get a free quote

CNY 4,466.00


货期*
5周

规格
    • 100 ug

Product images

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.
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).
Reference Data
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
Customer Reviews 
Loading...