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Alexa Fluor® 488 Rat Anti-Mouse CD45 Antibody (S-R477)

Alexa Fluor® 488 Rat Anti-Mouse CD45 Antibody (S-R477)

Catalog Number: S0B1600 Application: FCM Reactivity: Mouse Conjugation: Alexa Fluor 488 Brand: Starter
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Regular price $135 USD
Regular price Sale price $135 USD
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Product Details

Product Specification


Host Rat
Antigen Mouse CD45
Synonyms Receptor-type tyrosine-protein phosphatase C, Leukocyte common antigen (L-CA), T200, PTPRC
Location Cell membrane
Accession P06800
Clone Number S-R477
Antibody Type Rat mAb
Isotype IgG2b,k
Application FCM
Reactivity Ms
Purification Protein G
Concentration 0.2 mg/ml
Conjugation Alexa Fluor® 488
Physical Appearance Liquid
Storage Buffer

PBS, 25% Glycerol, 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 1.25μl 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 Mouse CD45 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with either Alexa Fluor® 488 Rat IgG2b Isotype Control (Black line histogram) or SDT Alexa Fluor® 488 Rat Anti-Mouse CD45 Antibody (Red line histogram) at 1.25 μl/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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