Anti-CD7 Antibody

Cat# CPA8551-30ul

Size : 30ul

Brand : Cohesion Biosciences

Contact local distributor :


Phone : +1 850 650 7790

  • Flow cytometric analysis of human peripheral blood lymphocytes using Anti-CD7 Antibody, followed by anti-mouse IgG PE.
Product Name:Anti-CD7 Antibody
Cat No:CPA8551
Source:Mouse
Reactivity:H
Applications:IF/IC, FC
*Application Key:
H - Human, M - Mouse, R - Rat, B - Bovine, C - Chicken, D - Dog, G - Goat, Mk - Monkey, P - Pig, Rb - Rabbit, S - Sheep, Z - Zebrafish
*Species Reactivity Key:
E- ELISA, WB - Western blot, IH - Immunohistochemistry, IF - Immunofluorescence, FC - Flow cytometry, IC - Immunocytochemistry, IP - Immunoprecipitation, ChIP - Chromatin Immunoprecipitation, EMSA - Electrophoretic Mobility Shift Assay, BL - Blocking, SE - Sandwich ELISA, CBE - Cell-based ELISA, RNAi - RNA interference
Description:Mouse monoclonal antibody to CD7
Immunogen:Native purified human CD7.
Purification:The antibody was purified by affinity chromatography.
Specificity:Recognizes human CD7
Clonality:Monoclonal (clone: T3-3A1)
Form:Mouse IgG1. Liquid in PBS, pH 7.3, and 0.02% sodium azide.
Dilution:IF/IC (1/50 - 1/200), FC (1/500 - 1/2000)
Gene Symbol:CD7
Alternative Names:T-cell antigen CD7; GP40; T-cell leukemia antigen; T-cell surface antigen Leu-9; TP41; CD antigen CD7
Entrez Gene (Human): 924;
SwissProt (Human): P09564;
Directions for Use:1. Take 100 μl peripheral blood anticoagulated by EDTA and add to the bottom of 5 ml tube. 2. Add appropriate amount of antibody to the bottom of flow tube mixing with the whole blood; incubate for 30 minutes at room temperature. 3. Add 2 ml RBC lysis buffer; incubate for 10 minutes after mixing; dissolve red blood cells. 4. Sample tube is set to 1000 rpm centrifugation for 5 minutes; discard the supernatant. 5. Add 2 ml PBS wash buffer to resuspend the cells; then 1000 rpm centrifugation for 5 minutes; discard the supernatant. 6. Add appropriate amount of fluorescent-labeled secondary antibody and incubate for 20 minutes away from light at room temperature. 7. Add 2 ml PBS wash buffer to resuspend the cells; then 1000 rpm centrifugation for 5 minutes; discard the supernatant. 8. Add 0.5 ml PBS wash buffer to resuspend the cells and detect by flow cytometry (sample should be determined on the day on the machine and can also be added fixation overnight at 4 °C then measured).
Storage/Stability:Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.