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Location: Home > Antigen, Antibodies, ELISA, Western Blot > Primary Antibody > Polyclonal Antibodies > Human Protease-activated Receptor-1 (extracellular) Antibody

Human Protease-activated Receptor-1 (extracellular) Antibody

Catalog # Availability Size / Price Inquiry
APR00491G 50 μl / $695

Human Protease-activated Receptor-1 (extracellular) Antibody

Brand

Leading Biology

Catalog Number

APR00491G

Product Type

Polyclonal Antibodies

Field of Research

Product Overview

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality Human Protease-activated Receptor-1 (extracellular) Antibody.

Molecular Weight

47441 Da

Host

Rabbit

Species Reactivity

Human

Target

Peptide (C)KNESGLTEYRLVSINK, corresponding to amino acid residues 61-76 of human PAR-1 (Accession P25116). Extracellular, N terminal.Unlikely to recognize mouse or rat samples.

GeneID

UniProt ID

Summary

Protease-activated receptor 1 (PAR-1) belongs to a family of four G protein-coupled receptors (PAR-1 - 4) that are activated as a result of proteolytic cleavage by certain serine proteases, hence their name. In this novel modality of activation, a specific protease cleaves the PAR receptor within a defined sequence in its extracellular N-terminal domain. This results in the creation of a new N-terminal tethered ligand, which subsequently binds to a site in the second extracellular loop of the same receptor. This binding results in the coupling of the receptor to G proteins and in the activation of several signal transduction pathways.1-3 Different PARs are activated by different proteases. Hence, PAR-1 is activated by thrombin (and is in fact also known as the thrombin receptor), as are PAR-3 and PAR-4, while PAR-2 is activated by trypsin.1-3 PAR-1 can be also cleaved and activated by other proteases such as plasmin, Factor Xa, cathepsin G, and others. The intramolecular nature of PAR activation and the continuous presence of the tethered ligand that cannot diffuse away imply the existence of several mechanisms for the rapid termination of PAR signaling. Indeed, following receptor activation, there is rapid phosphorylation of the C-terminal end of the receptor, followed by receptor internalization and degradation. In addition, several proteases can cleave away the tethered ligand, thereby “disarming” the PAR.1-3 PAR-1 signals through several G proteins including Gaq, Gai, and Ga12/13, resulting in the activation of several transduction pathways including intracellular Ca2+ mobilization, Rho and Rac signaling, and MAPK activation.1-3 PAR-1 is expressed in several cell types including platelets, leukocytes, vascular endothelial cells, gastrointestinal epithelial cells, myocytes, and neurons. The best studied physiological function of PAR-1 is its involvement in the coagulation cascade. Thrombin, the preeminent ligand of PAR-1, activates the receptor on the surface of platelets, hence inducing platelet aggregation, granular secretion, and procoagulant activity. PAR-1 also plays a crucial role in vascular ontogenesis. Accordingly, PAR-1 knockout mice show bleeding at multiple sites and usually die at mid-gestation.1-3 PAR-1 also plays important roles in tumor growth and metastasis. PAR-1 is upregulated in several human cancers as are several proteases such as plasmin and matrix metalloproteases (MMPs) that act as PAR-1 ligands, thereby creating an autocrine loop. PAR-1 activation in cancer cells transmits mitogenic signals through the activation of the erk1/2 pathway and is involved in tumor spread via its pro-angiogenic activity.4 Abgent is pleased to offer a highly specific antibody directed against an epitope at the extracellular N-terminus of the human protease-activated receptor-1. Anti-Human Protease-Activated Receptor-1 (extracellular) antibody (#AG1059) can be used in western blot analysis, immunohistochemical, immunocytochemical, and flow cytometry applications. It has been designed to recognize PAR-1 from human samples.

Form

Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

Storage & Stability

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

Applications

WB, IHC, FC, ICC, LCI

Dilution

WB~~1:200-1:2000 IHC~~1:100 ICC~~1:50 IF~~1:20

Images

Western blot analysis of human promyelocytic leukemia HL-60 (lanes 1 and 4), human T-cell leukemia Jurkat (lanes 2 and 5), and chronic myelogenous leukemia K562 (lanes 3 and 6) cell line lysates: 1-3. Anti-Human Protease-Activated Receptor-1 (extracellular) antibody (APR00491G), (1:200). 4-6. Anti-Human Protease-Activated Receptor-1 (extracellular) antibody, preincubated with the control peptide antigen.

Western blot analysis of human colon cancer HT-29 (lanes 1 and 3) and Colo-205 (lanes 2 and 4) cell line lysates: 1, 2. Anti-Human Protease-Activated Receptor-1 (extracellular) antibody (APR00491G), (1:200). 3, 4. Anti-Human Protease-Activated Receptor-1 (extracellular) antibody, preincubated with the control peptide antigen.

Expression of PAR-1 in normal human breast and human breast carcinoma Immunohistochemical staining of paraffin-embedded human breast sections using Anti-Human Protease-Activated Receptor-1 (extracellular) antibody (APR00491G), (1:100). PAR-1 staining is highly specific for epithelium-derived cells. A. In the normal resting breast, epithelial cells of the mammary ducts are visible using Histofine (pink). B. The breast carcinoma contains epithelium-derived malignant cells stained with DAB (brown). Hematoxilin is used as the counterstain.

Specification

Quantity

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