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Mouse PD-1 Alexa Fluor 488 MAb (Clone 766104)  100 TESTS图1

Mouse PD-1 Alexa Fluor 488 MAb (Clone 766104) 100 TESTS

2024-11-24 17:47IP属地 广东省东莞市 电信00留言

Applications

Please Note: Optimal dilutions should be determined by each laboratory for each application.  are available in the Technical Information section on our website.

Data Examples

Flow Cytometry      
     

Detection of PD‑1 in Mouse Splenocytes by Flow Cytometry. Mouse splenocytes either (A) resting or (B) treated with 5 μg/mLof PHA for 72 hours were stained with Rat Anti-Mouse PD‑1 Alexa Fluor® 488‑conjugated Monoclonal Antibody (Catalog # FAB7738G, filled histogram) or isotype control antibody (Catalog # , open histogram). View our protocol for . 

Flow Cytometry      
     

Detection of PD‑1 in Mouse Thymocytes by Flow Cytometry. Mouse thymocytes gated on CD3+ CD8+ cells were stained with Rat Anti-Mouse CD4 Alexa Fluor® 405‑conjugated Monoclonal Antibody (Catalog # ) and either (A) Rat Anti-Mouse PD‑1 Alexa Fluor® 488‑conjugated Monoclonal Antibody (Catalog # FAB7738G) or (B) Rat IgG2A Alexa Fluor 488 Isotype Control (Catalog # ). View our protocol for .

Preparation and Storage

Background: PD-1

Programmed Death-1 (PD-1) is a type I transmembrane protein belonging to the CD28/CTLA-4 family of immunoreceptors that mediate signals for regulating immune responses (1). Other members of this family include CD28, CTLA-4, and ICOS (2-4). PD-1 is most closely related to CTLA-4 and shares approximately 24% amino acid (aa) sequence identity. The mouse PD-1 gene encodes a 288 aa protein with a putative 20 aa signal peptide, a 149 aa extracellular region with one immunoglobulin-like V-type domain, a 21 aa transmembrane domain, and a 98 aa cytoplasmic region. The cytoplasmic tail contains two tyrosine residues that form the immunoreceptor tyrosine-based inhibitory motif (ITIM) and immunoreceptor tyrosine-based switch motif (ITSM) that are important in mediating PD-1 signaling. Mouse and human PD-1 share approximately 69% aa sequence identity. Two B7 family proteins, PD-L1 (also called B7-H1) and PD-L2, have been identified as PD-1 ligands (5, 6). PD-1 is expressed on activated T cells, B cells, myeloid cells, and on a subset of thymocytes. PD-1 deficient mice have a defect in peripheral tolerance and spontaneously develop autoimmune diseases. Binding of PD-1 to PD-L1 or PD-L2 results in the inhibition of TCR-mediated proliferation and cytokine production as well as BCR-mediated signaling. PD-1 likely has an inhibitory role in regulating immune responses (1-4).

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