Cynomolgus / Rhesus macaque PD-L1 / B7-H1 Protein, His Tag

Proteins and Peptides

貨號 Cat. No.
PD1-C52H4
規格 Size
100ug
品牌 Brand
ACROBiosystems
Species
Cynomolgus / Rhesus macaque
Conjugate
Unconjugated
Expression System
HEK293
Tag
His Tag

Description




Source : 


Cynomolgus / Rhesus macaque PD-L1, His Tag (PD1-C52H4) is expressed from human 293 cells (HEK293). It contains AA Phe 19 - Arg 238 (Accession # G7PSE7-1). In the region Phe 19 - Arg 238, the AA sequence of Cynomolgus and Rhesus macaque PD-L1 are homologus.


 

Molecule : PD-L1


 

Synonyms : PD-L1,CD274,B7-H1,PDCD1L1,PDCD1LG1


 

Format : Powder


 

Category : Immune Checkpoint Proteins


 

Accession : N/A


 

Storage : -20℃


 

Shipping condition : Powder,RT


 

Molecular Weight : 27.1 kDa


 

Characteristics :


This protein carries a polyhistidine tag at the C-terminus. The protein has a calculated MW of 27.1 kDa. The protein migrates as 37-42 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.


 

Endotoxin Level : Less than 1.0 EU per μg by the LAL method.


 

Buffer : PBS, pH7.4


 

Description :


Programmed cell death 1 ligand 1 (PDL1) is also known as B7-H, B7H1, MGC142294, MGC142296, PD-L1, PDCD1L1 and PDCD1LG1,which is a member of the growing B7 family of immune molecules and is involved in the regulation of cellular and humoral immune responses.PDL1 is a cell surface immunoglobulin superfamily with two Ig-like domains within the extracellular region and a short cytoplasmic domain. This protein is broadly expressed in the majority of peripheral tissues as well as hematopoietic cells. Interaction between PDL1 and its receptors belonging to the CD28 family of molecules provide both stimulatory and inhibitory signals in regulating T cell activation and tolerance. PDL1 may inhibit ongoing T-cell responses by inducing apoptosis and arresting cell-cycle progression.


 

References :


(1) Dong H., et al., 1999, Nat. Med. 5:1365-1369.
(2) Freeman G.J., et al., 2000, J. Exp. Med. 192:1027-1034.
(3) Nishimura H., et al., 2001, Trends in Immunology 22:265. 





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