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- Order number: 7TM0218N
- Content: 100 µl
- Host: Rabbit
The non-phospho-Dopamine Receptor 5 Antibody is directed against the distal end of the carboxyl-terminal tail of human D5. It can be used to detect total D5 receptors in Western blots independent of phosphorylation. The non-phospho-D5 antibody can also be used to isolate and enrich D5 receptors from cell and tissue lysates. It also detects D5 in cultured cells and tissue sections by immunohistochemistry.
| Alternative Names | D5, DRD1B, Dopamine Receptor 5, D(1B)Dopamine Receptor |
| IUPHAR Target ID | 218 |
| UniProt ID | P21918 |
| Western Blot (WB) | 1:1000 |
| Immunohistochemistry (IHC) | 1:100 |
| Species Reactivity | Human, Mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Immunogen | A synthetic peptide presents carboxyl-terminal tail of human D5. |
| 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 Dopamine Receptor 5 in transfected HEK293 cells. Native HEK293 cells (MOCK) or HEK293 cells stably expressing the dopamine receptor 5 (D5) were lysed and immunoblotted with the phosphorylation-independent anti-D5 antibody (7TM0218N) at a dilution of 1:1000.
Figure 2. Immunohistochemical identification of Dopamine Receptor 5 in mouse hippocampus. Sections were dewaxed, microwaved in citric acid, and incubated with anti-D5 (Dopamine Receptor 5) antibody (7TM0218N) 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.
Figure 3. Immunohistochemical identification of Dopamine Receptor 5 in human cortex. Sections were dewaxed, microwaved in citric acid, and incubated with anti-D5 (Dopamine Receptor 5) antibody (7TM0218N) 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.
Figure 4. Immunohistochemical varification of Dopamine Receptor 5 antibody in human cortex. Sections were dewaxed, microwaved in citric acid, and not exposed (left pannel) or exposed to peptide (right pannel) that was used for production of anti-D5 (non-phospho-Dopamine Receptor 5) antibody (7TM0218N). Sections were then incubated with anti-D5 (non-phospho-Dopamine Receptor 5) antibody (7TM0218N) at a dilution of 1:100 and 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. Note, only in sections without peptide incubation D5 receptors were uniformly detected at the plasma membrane of nearly all cells.
Figure 5. Immunohistochemical varification of Dopamine Receptor 5 antibody in rat cortex. Sections were dewaxed, microwaved in citric acid, and not exposed (left pannel) or exposed to peptide (right pannel) that was used for production of anti-D5 (non-phospho-Dopamine Receptor 5) antibody (7TM0218N). Sections were then incubated with anti-D5 (non-phospho-Dopamine Receptor 5) antibody (7TM0218N) at a dilution of 1:100 and 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. Note, only in sections without peptide incubation D5 receptors were uniformly detected at the plasma membrane of nearly all cells.



