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Alexa Fluor® 488 Rat Anti-Mouse/Human CD45R/B220 Antibody (S-R519)

Alexa Fluor® 488 Rat Anti-Mouse/Human CD45R/B220 Antibody (S-R519)

Catalog Number: S0B5952 Application: FCM Reactivity: Human,Mouse Conjugation: Alexa Fluor® 488 Brand: Starter
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Regular price $79.00 SGD
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Product Details

Product Specification


Host Rat
Antigen CD45R/B220
Synonyms Receptor-type tyrosine-protein phosphatase C; Leukocyte common antigen (L-CA); Lymphocyte antigen 5 (Ly-5); T200; CD45; Ly-5; Ptprc
Location Cell membrane, Synapse
Accession P06800
Clone Number S-R519
Antibody Type Rat mAb
Isotype IgG2a,k
Application FCM
Reactivity Hu, Ms
Positive Sample BALB/c mouse splenocytes
Purification Protein G
Concentration 0.2 mg/ml
Conjugation Alexa Fluor® 488
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 5μl per million cells in 100μl volume Ms

Background

CD45R/B220 is an isoform of the CD45 protein, a member of the protein tyrosine phosphatase (PTP) family, and serves as a critical regulator of T- and B-cell antigen receptor signaling. It is predominantly expressed on the surface of B cells, from early pro-B cells to mature and activated B cells, making it a commonly used pan-B cell marker in mice. Additionally, CD45R/B220 is also found on certain subsets of activated T cells, lymphokine-activated killer cells (LAK), NK cell progenitors, and T cells in mutant mice. This molecule plays a crucial role in lymphocyte development and antigen signaling, and its expression is regulated during different stages of B cell maturation.

Picture

FC

Flow cytometric analysis of CD45R/B220 expression on BALB/c mouse splenocytes. BALB/c mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 Antibody and either Alexa Fluor® 488 Rat IgG2a, κ Isotype Control (Left panel) or Alexa Fluor® 488 Rat Anti-Mouse/Human CD45R/B220 Antibody (Right panel) at 5μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.