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APC-Cy7 Mouse Anti-Human CD45 Antibody (S-839-3)

APC-Cy7 Mouse Anti-Human CD45 Antibody (S-839-3)

Catalog Number: S0B1583 Application: FCM Reactivity: Human Conjugation: APC-Cy7 Brand: Starter
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Regular price $156.00 SGD
Regular price Sale price $156.00 SGD
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Product Details

Product Specification


Host Mouse
Antigen CD45
Synonyms Receptor-type tyrosine-protein phosphatase C, Leukocyte common antigen (L-CA), T200, PTPRC
Immunogen Recombinant Protein
Location Cell membrane
Accession P08575
Clone Number S-839-3
Antibody Type Mouse mAb
Isotype IgG1,k
Application FCM
Reactivity Hu
Purification Protein G
Concentration 0.1mg/ml
Conjugation APC-Cy7
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.3% Proclin 300

Stability & Storage 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.

Dilution


application dilution species
FCM 2.5 μl per million cells in 100μl volume

Background

CD45 is a member of the protein tyrosine phosphatase (PTP) family. CD45 is a type I transmembrane protein that is present in various isoforms on all differentiated hematopoietic cells (except erythrocytes and plasma cells). CD45 has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes via its extracellular domain (a form of co-stimulation), or by activating various Src family kinases required for the antigen receptor signaling via its cytoplasmic domain. CD45 also suppresses JAK kinases, and so functions as a negative regulator of cytokine receptor signaling.

Picture

FC

Flow cytometric analysis of Human CD45 expression on human PBMC (human peripheral blood mononuclear cell). human PBMC were stained with either APC-Cy7 Mouse IgG1, κ Isotype Control (Black line histogram) or SDT APC-Cy7 Mouse Anti-Human CD45 Antibody (Red line histogram) at 0.25 μg/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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