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- Order number: 7TM0350N
- Content: 100 µl
- Host: Rabbit
The non-phospho-PAR4 receptor antibody is directed against the distal end of the carboxyl-terminal tail of human Proteinase-Activated Receptor 4. It can be used to detect total PAR4 receptors in Western blots independent of phosphorylation. The PAR4 antibody can also be used to isolate and enrich PAR4 receptors from cell and tissue lysates. It also detects PAR4 in cultured cells and tissue sections by immunohistochemistry.
Alternative Names | Coagulation Factor II Receptor-like 3, Protease-Activated Receptor 4, Thrombin receptor-like 3 |
IUPHAR Target ID | 350 |
UniProt ID | Q96RI0 |
Western Blot (WB) | 1:1000 |
Immunohistochemistry (IHC) | 1:100 |
Species Reactivity | Human |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Immunogen | A synthetic peptide presents distal part of carboxyl-terminal tail of human PAR4. |
Form | Liquid |
Purification | Antigen affinity chromatography |
Storage buffer | Dulbecco's PBS, pH 7.4, with 150 mM NaCl, 0.02% sodium azide |
Storage conditions | short-term 4°C, long-term -20°C |
Figure 1. Validation of the Proteinase-Activated Receptor 4 in transfected HEK293 cells. Native HEK293 cells (MOCK) or HEK293 cells stably expressing the Proteinase-Activated Receptor 4 (PAR4) were lysed and immunoblotted with the anti-PAR4 antibody (7TM0350N) at a dilution of 1:1000.
Figure 2. Immunohistochemical identification of Proteinase-Activated Receptor 4 in Small Intestine. Sections were dewaxed, microwaved in citric acid, and incubated with anti-PAR4 (PAR4 Receptor) antibody (7TM0350N) at a dilution of 1:100. Sections were then sequentially treated with biotinylated anti-rabbit IgG and avidin-biotin solution. Sections were then developed in 3,3-diaminobenzidine (DAB)-glucose oxidase and lightly counterstained with hematoxylin.