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Alexa Fluor® 647 Rat Anti-Mouse CD22 Antibody (OX-97)

Alexa Fluor® 647 Rat Anti-Mouse CD22 Antibody (OX-97)

Catalog Number: S0B80619 Application: FCM Reactivity: Ms Conjugation: Alexa Fluor® 647 Brand: Starter
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Regular price $85 USD
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Product Details

Product Specification


Host Rat
Antigen CD22
Synonyms B-cell receptor CD22; B-lymphocyte cell adhesion molecule (BL-CAM); Sialic acid-binding Ig-like lectin 2 (Siglec-2); T-cell surface antigen Leu-14; Lyb-8; Siglec2; Cd22
Location Cell membrane
Accession P35329
Clone Number OX-97
Antibody Type Rat mAb
Isotype IgG1,k
Application FCM
Reactivity Ms
Positive Sample C57BL/6 mouse splenocytes
Purification Protein G
Concentration 0.5 mg/ml
Conjugation Alexa Fluor® 647
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 1μg per million cells in 100μl volume Ms

Background

CD22, also known as cluster of differentiation 22, is a 140 kDa type I transmembrane glycoprotein and a member of the Siglec (sialic acid-binding immunoglobulin-like lectin) family. It is predominantly expressed on the surface of mature B cells and to a lesser extent on some immature B cells. The extracellular domain of CD22 consists of seven immunoglobulin-like domains, while its cytoplasmic tail contains conserved tyrosine motifs, including immunoreceptor tyrosine-based inhibitory motifs (ITIMs), which play a crucial role in inhibiting B cell receptor (BCR) signaling. CD22 functions as a negative regulator of B cell activation, helping to prevent overactivation of the immune system and the development of autoimmune diseases. Additionally, it is involved in B cell trafficking and maintaining peripheral B cell tolerance. CD22's interaction with sialic acid-containing molecules on various cell types allows it to modulate B cell responses and maintain immune homeostasis.

Picture

FC

Flow cytometric analysis of CD22 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 Antibody and either Alexa Fluor® 647 Rat IgG1, κ Isotype Control (left panel) or SDT Alexa Fluor® 647 Rat Anti-Mouse CD22 Antibody (right panel) at 2 μl/test. Total viable cells, as determined by Fixable Viability Dye 515 (S0B88804), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.