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ELK Biotechnology
SKU:ES2274
EphB6 Rabbit Polyclonal Antibody
EphB6 Rabbit Polyclonal Antibody
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$248.00 USD
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EphB6 Rabbit Polyclonal Antibody
Overview
| Product name: | EphB6 rabbit pAb |
| Alternative Names: | EPHB6; Ephrin type-B receptor 6; HEP; Tyrosine-protein kinase-defective receptor EPH-6 |
| Applications: | WB;IHC;IF;ELISA |
| Recommended Dilutions: | Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/5000. Not yet tested in other applications. |
| Immunogen: | The antiserum was produced against synthesized peptide derived from human EPHB6. AA range:861-910 |
| Storage: | Rabbit |
| Storage: | -20°C/1 year |
| Clonality: | Polyclonal |
| Isotype: | IgG |
| Concentration: | 1 mg/ml |
| Observed Band: | 119kD |
| GeneID(Human): | 2051 |
| Human Swiss-Prot No: | O15197 |
| Cellular localization: | Membrane; Single-pass type I membrane protein.; [Isoform 3]: Secreted . |
| Background: | This gene encodes a member of a family of transmembrane proteins that function as receptors for ephrin-B family proteins. Unlike other members of this family, the encoded protein does not contain a functional kinase domain. Activity of this protein can influence cell adhesion and migration. Expression of this gene is downregulated during tumor progression, suggesting that the protein may suppress tumor invasion and metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013], |
| Species Reactivity: | Human;Mouse;Rat |
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Western Blot analysis of various cells using EphB6 Polyclonal Antibody -
Immunofluorescence analysis of HeLa cells, using EPHB6 Antibody. The picture on the right is blocked with the synthesized peptide. -
Immunohistochemistry analysis of paraffin-embedded human brain tissue, using EPHB6 Antibody. The picture on the right is blocked with the synthesized peptide. -
Western blot analysis of lysates from COLO, 293, and HeLa cells, using EPHB6 Antibody. The lane on the right is blocked with the synthesized peptide.
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