Background：FAP (also known as seprase) is a Type II transmembrane serine protease.
Both plasma membrane and soluble forms exhibit post-proline cleaving endopeptidase activity, with a marked preference for Ala/Ser-Gly-Pro-Ser/Asla consensus sequences.
Degrade also gelatin, heat-denatured type I collagen.
Also has dipeptidyl peptidase activity, with a preference for Ala-Pro, Ile-Pro, Gly-Pro, Arg-Pro and Pro-Pro.
The plasma membrane form, in association with either DPP4, PLAUR or integrins, is involved in the pericellular proteolysis of the extracellular matrix (ECM), and hence promotes cell adhesion, migration and invasion through the ECM.
Promotes glioma cell invasion through the brain parenchyma by degrading the proteoglycan brevican.
Acts as a tumor suppressor in melanocytic cells through regulation of cell proliferation and survival in a serine protease activity-independent manner.
仕様
サイズ：25ug
Source：FITC-Labeled Human FAP, Fc Tag (FAP-HF263) is expressed from human 293 cells (HEK293). It contains AA Leu 26 - Asp 760 (Accession # Q12884-1). It is the FITC labeled form of Human FAP, Fc Tag (FAP-H5263).
Molecule：FAP
Synonyms：FAP,FAPalpha,SIMP,Seprase,APCE
Species：Human
Tag：Fc Tag
Expression Systems：HEK293
Expression Rigeion：Leu 26 - Asp 760
Conjugate：FITC Labeled Protein
Accession：NP_004451.2
Molecular Weight：111.5 kDa
Characteristics：This protein carries a human IgG1 Fc tag at the N-terminus. The protein has a calculated MW of 111.5 kDa. The protein migrates as 110-130 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.
Endotoxin Level：Less than 1.0 EU per ug by the LAL method.
