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PE-Cy7 Rat Anti-Mouse Ter-119/Erythroid Cells Antibody (S-R517)

PE-Cy7 Rat Anti-Mouse Ter-119/Erythroid Cells Antibody (S-R517)

Catalog Number: S0B8020 Application: FCM Reactivity: Mouse Conjugation: PE-Cy7 Brand: Starter
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Regular price $92.00 SGD
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Product Details

Product Specification


Host Rat
Antigen Mouse Ter-119
Synonyms Lymphocyte antigen 76; Ly76; Ly-76; Ter119
Location Cell membrane
Clone Number S-R517
Antibody Type Rat mAb
Isotype IgG2b,k
Application FCM
Reactivity Ms
Positive Sample C57BL/6 mouse bone marrow
Purification Protein G
Concentration 0.2 mg/ml
Conjugation PE-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 1.25μl per million cells in 100μl volume Ms

Background

The TER-119 protein is one of the most specific and important cell surface markers for the murine erythroid lineage. It specifically recognizes an antigen associated with glycophorin A on the red blood cell membrane. Throughout erythroid development, from early basophilic erythroblasts to late-stage reticulocytes, it is consistently highly expressed, making it a critical molecular marker for identifying, sorting, and studying murine erythroid cells (such as erythrocytes, progenitor cells, and precursors). This protein belongs to the Ly-6 antigen superfamily, and its antibody (e.g., the TER-119 monoclonal antibody) is an indispensable tool in experimental hematology for the isolation and identification of red blood cells via flow cytometry or immunomagnetic beads, as well as for research into blood diseases like anemia and leukemia.

Picture

FC

Flow cytometric analysis of Mouse TER-119/Erythroid expression on C57BL/6 mouse bone marrow. C57BL/6 mouse bone marrow were stained with Alexa Fluor® 488 Rat Anti-Mouse CD45 antibody and SDT PE-Cy7 Rat Anti-Mouse Ter-119/Erythroid Cells Antibody at 1.25 μl/test treated with True-Stain Monocyte Blocker™. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.