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The protein encoded by DPP4 is a homodimeric integral membrane gelatinase belonging to the serine protease family. Additionally we are shipping DPP4 Kits (73) and DPP4 Proteins (54) and many more products for this protein.
Showing 10 out of 620 products:
Human Monoclonal DPP4 Primary Antibody for FACS, IHC (p) - ABIN1106157
Kotani, Asada, Aratake, Umeki, Yamamoto, Tokudome, Hirai, Kuma, Konoe, Araki: Diagnostic usefulness of dipeptidyl aminopeptidase IV monoclonal antibody in paraffin-embedded thyroid follicular tumours. in The Journal of pathology 1993
Show all 4 references for ABIN1106157
Mouse (Murine) Monoclonal DPP4 Primary Antibody for FACS - ABIN320274
Cinar, Senol, Ozen: Immunohistochemical study on distribution of endocrine cells in gastrointestinal tract of flower fish (Pseudophoxinus antalyae). in World journal of gastroenterology : WJG 2006
Show all 3 references for ABIN320274
Human Polyclonal DPP4 Primary Antibody for IHC (p) - ABIN188903
Amatya, Takeshima, Kushitani, Yamada, Morimoto, Inai: Overexpression of CD26/DPPIV in mesothelioma tissue and mesothelioma cell lines. in Oncology reports 2011
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Dog (Canine) Polyclonal DPP4 Primary Antibody for EIA, WB - ABIN374762
Pei, Li, von Geldern, Longenecker, Pireh, Stewart, Backes, Lai, Lubben, Ballaron, Beno, Kempf-Grote, Sham, Trevillyan: Discovery and structure-activity relationships of piperidinone- and piperidine-constrained phenethylamines as novel, potent, and selective dipeptidyl peptidase IV inhibitors. in Journal of medicinal chemistry 2007
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Human Monoclonal DPP4 Primary Antibody for FACS, IF - ABIN2452961
Zhao, Li, Wohlford-Lenane, Agnihothram, Fett, Zhao, Gale, Baric, Enjuanes, Gallagher, McCray, Perlman: Rapid generation of a mouse model for Middle East respiratory syndrome. in Proceedings of the National Academy of Sciences of the United States of America 2014
Show all 2 references for ABIN2452961
Mouse (Murine) Monoclonal DPP4 Primary Antibody for EIA, FACS - ABIN120302
Vivier, Marguet, Naquet, Bonicel, Black, Li, Bernard, Gorvel, Pierres: Evidence that thymocyte-activating molecule is mouse CD26 (dipeptidyl peptidase IV). in Journal of immunology (Baltimore, Md. : 1950) 1991
Human Monoclonal DPP4 Primary Antibody for FACS - ABIN118573
Berg, James, Alvarez-Iglesias, Glennie, Lechler, Marelli-Berg: Functional consequences of noncognate interactions between CD4+ memory T lymphocytes and the endothelium. in Journal of immunology (Baltimore, Md. : 1950) 2002
The level of FAP expression in NGP-127, SJCRH30, and SJSA-1 lines as well as in cancer-associated fibroblasts of patients was comparable, which makes these cell lines a possible model for studying FAP
hypoxia altered the expression of DPP4 in human preadipocytes
High CXCL9 (show CXCL9 Antibodies) plasma levels favour response to pegIFN alpha 2a and ribavirin in hepatitis C virus infected patients regardless of DPP4 activity.
increased DPP4 activities are strongly and independently associated with diabetic nephropathy in type 2 diabetes
High stromal CD26 expression is associated with rectal cancer.
Serum DPP-4 levels were positively associated with visceral fat obesity and metabolic syndrome in men with type 2 diabetes mellitus.
Data show that high level of serum dipeptidyl peptidase-4 (DPP-4) is associated with multiple vertebral fractures (VFs) independently of bone mineral density (BMD (show BEST1 Antibodies)) and bone formation in men with type 2 diabetes mellitus (T2DM).
DPP4 may be involved in the pathologic features of asthmatic airway inflammation and cell proliferation and FN production.
NPY is efficiently cleaved by FAP indicating a potential function for FAP in neuropeptide regulation within liver and cancer biology.
degradomic study highlights cell-contextual proteolysis by FAPalpha with distinct positional profiles. Generally, our findings link FAPalpha to key aspects of CAF (show KAT2B Antibodies) biology and attribute an important role in tumor-stroma interaction to FAPalpha
Results describe a proline-rich cytokine from neurosecretory granules that represents a new natural substrate for Dipeptidyl Peptidase IV (DPPIV).
Data demonstrate that dipeptidyl peptidase II (show DPP7 Antibodies) can form a complex with adenosine deaminase (show ADA Antibodies), but with one order of magnitude higher dissociation constant than that of DPPIV.
This study shows that porcine DPP-IV is generally inhibited with greater potency by protein-derived peptides than is the human enzyme
DPP-IV from porcine kidney cortex was characterized.
Neutral endopeptidase 24.11 (show MME Antibodies) and DPP-IV is superior to DPP-IV inhibition alone in preserving intact GLP-1 (show GCG Antibodies), which implies possibility that the combination has therapeutic potential.
Results describe the distribution of dipeptidyl peptidase IV-like activity enzymes in porcine tissue sections by RT-PCR.
DPP4 posttranslational modification of selected chemokines by truncation modifies their functional activities.
DPP (show DSPP Antibodies)-4I, MK0626, but not native incretins has protective effects against AAA (show AAAS Antibodies) in Ang II (show AGT Antibodies)-infused Apoe (show APOE Antibodies)/ mice via suppression of inflammation, proteolysis, and fibrosis in the aortic wall
Plasminogen (show PLG Antibodies) may regulate DPP-4 activity and glucose metabolism.
DPP-4 inhibition may have direct protective effects on the post-myocardial infarction heart by inducing an antiapoptotic effect and inhibiting a decrease in vessel number through the SDF-1a/CXCR4 (show CXCR4 Antibodies)-mediated STAT3 (show STAT3 Antibodies) signaling pathway.
Data suggest that pharmacological stimulation of serotonin 5Ht1b (show HTR1B Antibodies) receptor enhances up-regulation of plasma Glp1 (glucagon-like peptide 1 (show GCG Antibodies)) induced by Dpp4 (dipeptidylpeptidase 4) inhibition independently of feeding and also improves glucose tolerance.
Young euglycemic Dpp4 KO mice showed a cardioprotective response after transverse aortic constriction or doxorubicin administration, with reduced fibrosis; however, cardiac mRNA analysis revealed increased expression of inflammation-related transcripts.
Dipeptidyl peptidase-4 inhibition by gemigliptin exerts a preventative effect on the proliferation and migration of VSMCs via Nrf2 (show NFE2L2 Antibodies).
The present study reveals the activation of autophagy to mediate the anti-diabetic effect of GLP-1 (show GCG Antibodies).
These results indicate that DPP-4 inhibitors pleiotropically exert a direct renoprotective effect, and may serve as an additional therapeutic strategy to protect proximal tubular cells against proteinuria in patients with diabetic nephropathy.
DPP-4 and integrin beta1 interactions regulate key endothelial cell signal transduction in both physiological and pathological conditions including endothelial mesenchymal transformation.
The protein encoded by this gene is a homodimeric integral membrane gelatinase belonging to the serine protease family. It is selectively expressed in reactive stromal fibroblasts of epithelial cancers, granulation tissue of healing wounds, and malignant cells of bone and soft tissue sarcomas. This protein is thought to be involved in the control of fibroblast growth or epithelial-mesenchymal interactions during development, tissue repair, and epithelial carcinogenesis.
dipeptidyl peptidase 9
, dipeptidyl-peptidase 4
, dipeptidyl-peptidase IV
, dipeptidyl-peptidase 4 (CD26, adenosine deaminase complexing protein 2)
, dipeptidylpeptidase IV
, dipeptidyl peptidase 4
, DPP IV
, T-cell activation antigen CD26
, adenosine deaminase complexing protein 2
, dipeptidyl peptidase IV
, dipeptidylpeptidase 4
, dipeptidylpeptidase IV (CD26, adenosine deaminase complexing protein 2)
, activation molecule 3
, adenosine deaminase complexing protein
, dipeptidyl-peptidase iv
, thymocyte-activating molecule
, GP110 glycoprotein
, bile canaliculus domain-specific membrane glycoprotein
, 170 kDa melanoma membrane-bound gelatinase
, integral membrane serine protease