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FAP belongs to the serine protease family.
Showing 4 out of 4 products:
Adora2B (show ADORA2B Antibodies) stimulation promotes FGF2 (show FGF2 Antibodies) and CXCL12 (show CXCL12 Antibodies) expression in FAP-positive melanoma-associated (show ZNF654 Antibodies) fibroblasts, contributing to the creation of a tumor-promoting microenvironment.
There was no evidence of compensatory upregulation of other DPP4 (show DPP4 Antibodies) family members in influenza-infected FAP-deficient mice. FAP appears to be dispensable in anti-influenza adaptive immunity.
FAP-STAT3 (show STAT3 Antibodies)-CCL2 (show CCL2 Antibodies) signaling in Cancer-associated fibroblasts (CAF (show LAMA2 Antibodies)) was sufficient to program an inflammatory component of the tumor microenvironment, which may have particular significance in desmoplasia-associated cancers.
Taken together, our study suggested that high FAP expression in CAFs (show TBX1 Antibodies) is one reason leading to immune checkpoint blockades resistance in CRC (show SCRIB Antibodies) patients and FAP is an optional target for reversing immune checkpoint blockades resistance.
FAP-vaccinated mice also treated with Cyclophosphamide chemotherapy showed a marked suppression of tumor growth (inhibition ratio =80%) and a prolongation of survival time.
In two different models of pulmonary fibrosis, intratracheal bleomycin instillation and thoracic irradiation, the study finds increased mortality and increased lung fibrosis in FAP-deficient mice compared with wild-type mice.
Mouse FGF-21 (show FGF21 Antibodies), however, lacks the FAP cleavage site and is not cleaved by FAP.
Data indicate that indolamine-2,3-dioxygenase (IDO (show IDO1 Antibodies)) and Fibroblast activation protein alpha (FAPalpha) were detectable in B16 melanoma tumor-bearing mice.
A transgenic mouse model for pulmonary fibrosis was generated. After bleomycin induction, luciferase cDNA under the control of the FAPa promoter presents strong luminescence in the lungs especially; the expression level reflects the degree of the disease.
The FAP(+) stromal cell may have roles in two adverse consequences of cancer.
This gene belongs to the serine protease family. The encoded protein is an inducible cell-surface bound glycoprotein specifically expressed in tumor-associated fibroblasts and pericytes of epithelial tumors and has protease and gelatinase activity. The protein plays a role in remodeling of the extracellular matrix (ECM) and may affect tumorigenesis and tissue repair. Alternately spliced transcript variants of this gene are described in the literature (PMID 9139873), but the full-length sequence of these variants is not available.
fibroblast activation protein alpha
, integral membrane serine protease