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Mouse PD-1 ELISA Kit

$713.00

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Assay Range

125-8000 pg/mL  

Sensitivity

10.0 pg/mL

Specificity

No cross-reaction with other related substances detected

Size

96T

Storage

Store at 2 - 8ºC. Keep reconstituted standard and detection Ab at -20 ºC

Assay Principle

Sandwich ELISA

Sample Volume

100 µL final volume, dilution factor varies on samples

Sample Type

Cell culture supernatant 

Detection Method

Chromogenic

 

 

Kit Components

 

 1. Recombinant Mouse PD-1 standard: 2 vials

 2. One 96-well plate coated with Mouse PD-1  Ab

 3. Sample diluent buffer: 12 mL - 1

 4. Detection antibody: 1 vial

 5. Streptavidin-HRP:  1 vial

 6. Antibody diluent buffer: 12 mL x1   

 7. Streptavidin-HRP diluent buffer: 12 mL x1

8. Chromogenic Solution  A:  6 mlx1

 9. Chromogenic Solution  B:  6 mL x1

10. Stop solution: 6 mL x1

11. Washing solution (20x): 25 mL x1

 

 

Background

 

Programmed Death-1 (PD-1), also known as Programmed Cell Death-1, or CD279, is a type I transmembrane protein belonging to the CD28/CTLA-4 family. The human PD1 is synthesized as a 288 amino acid (aa) protein containing a putative 20 aa signal peptide, a 148 aa extracellular region with one immunoglobulin-like V-type domain, a 24 aa transmembrane domain and a 95 aa cytoplasmic region which consists of two tyrosine residues that form the immuno receptor tyrosine-based inhibitory motif (ITIM) and immunoreceptor tyrosine-based switch motif (ITSM) that play a role in mediating PD-1 signaling. PD-1 is expressed on activated T cells, B cells, myeloid cells and on a subset of thymocytes. Human PD-1 shares approximately 60% aa sequence identity with mouse counterpart.

PD-L1/B7H1 and PD-L2/B7DC, members of the B7 family, are the ligands for PD-1. PD-L1 protein is upregulated on macrophages and dendritic cells (DC) in response to LPS and GM-CSF treatment, and on T cells and B cells when TCR and B cell receptor is activated. PD-L1 is expressed on almost all murine tumor cell lines, such as PA1 myeloma, P815 mastocytoma, and B16 melanoma upon treatment with IFN-γ. PD-L2 is expressed mainly by DCs and a few tumor lines. It is reported that ligation of PD-1 inhibits TCR-mediated T cell proliferation and production of IL-1, IL-4, IL-10,and IFNγ, as well as BCR mediated signaling pathways. In addition, PD-1 deficient mice have shown a defect in peripheral tolerance and spontaneously develop autoimmune diseases, suggesting that PD-1 might play a role in the regulation of peripheral tolerance and in preventing autoimmune diseases.

 

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