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PE-Cy7 Mouse Anti-Mouse CD45.1 Antibody (A20)

PE-Cy7 Mouse Anti-Mouse CD45.1 Antibody (A20)

Catalog Number: S0B80945 Application: FCM Reactivity: Ms Conjugation: PE-Cy7 Brand: Starter
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Regular price $85 USD
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Product Details

Product Specification


Host Mouse
Antigen CD45.1
Location Cell membrane
Accession P06800
Clone Number A20
Antibody Type Mouse mAb
Application FCM
Reactivity Ms
Positive Sample SJL mouse splenocytes
Purification Protein A
Concentration 0.2 mg/ml
Conjugation PE-Cy7
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.09% sodium azide

Stability & Storage

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

Dilution


application dilution species
FCM 0.25μg per million cells in 100μl volume Ms

Background

CD45.1 is a protein isoform of CD45, also known as PTPRC, which is a receptor-type tyrosine phosphatase expressed on all hematopoietic cells except erythrocytes and platelets. This type I transmembrane protein plays a crucial role in the activation processes of B and T cell receptors, as well as in thymic selection. CD45.1, along with CD45.2, is commonly used in adoptive cell transfer experiments to distinguish donor cells from host cells due to their allelic differences. Mice carrying the CD45.1 allele, such as C57BL/6J, are widely used in research for this purpose. CD45.1 is also used in studies to understand the rejuvenating effects of young blood on aged tissues. In heterochronic parabiosis models, where the circulatory systems of old and young mice are connected, CD45.1 and CD45.2 genotypes are used to track the cells of old and young mice, respectively.

Picture

FC

Flow cytometric analysis of Mouse CD45.1 expression on SJL mouse splenocytes. SJL mouse splenocytes were stained either PE-Cy7 Mouse IgG2a, κ Isotype Control (left panel) or SDT PE-Cy7 Mouse Anti-Mouse CD45.1 Antibody (right panel) at 1.25 μl/test treated with True-Stain Monocyte Blocker™. Total viable cells, as determined by Fixable Viability Dye 452 (S0B88801), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.