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Biotin Mouse Anti-Human CD163 Antibody (S-3028)

Biotin Mouse Anti-Human CD163 Antibody (S-3028)

Catalog Number: S0B5910 Application: FCM Reactivity: Human Conjugation: Biotin Brand: Starter
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Regular price $131.00 SGD
Regular price Sale price $131.00 SGD
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Product Details

Product Specification


Host Mouse
Antigen CD163
Synonyms Scavenger receptor cysteine-rich type 1 protein M130; Hemoglobin scavenger receptor; M130
Location Secreted, Cell membrane
Accession Q86VB7
Clone Number S-3028
Antibody Type Mouse mAb
Isotype IgG1,k
Application FCM
Reactivity Hu
Positive Sample Human PBMC
Purification Protein G
Concentration 0.2 mg/ml
Conjugation Biotin
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 Hu

Background

CD163 is a type I membrane protein primarily expressed on the surface of monocytes and macrophages and belongs to the scavenger receptor cysteine-rich (SRCR) superfamily. It plays a crucial role in regulating immune responses and clearing heme proteins. CD163 binds to haptoglobin-hemoglobin complexes, facilitating iron recycling and protecting tissues from oxidative damage. As a marker of M2-type macrophages, CD163 is associated with anti-inflammatory functions by inhibiting the production of pro-inflammatory cytokines. In pathological conditions, the expression levels of CD163 are linked to various diseases, including inflammatory disorders, cancer, and viral infections. Soluble CD163 (sCD163) is often used as a biomarker for disease monitoring and assessment.

Picture

FC

Flow cytometric analysis of Human CD163 expression on Human PBMC. Human PBMC (peripheral blood mononuclear cells) were stained with Brilliant Violet 480™ Mouse Anti-Human CD14 Antibody and either Biotin Mouse IgG1, κ Isotype Control (Left panel) or Biotin Mouse Anti-Human CD163 Antibody (Right panel) at 5 μl/test followed by Sav-PE. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.