
Thermo Fisher Scientific Connexin 43 Recombinant Rabbit Monoclonal Antibody (105)
Connexin 43 단백질을 인식하는 재조합 토끼 단클론 항체로, 인간 시료에 반응합니다. IHC(P)에서 1:100–1:500 희석으로 사용 가능하며, PBS buffer에 보존됩니다. 단백질 A로 정제된 고순도 항체로 연구용으로 적합합니다.
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Applications
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:100–1:500
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | 105 |
| Immunogen | A synthetic peptide corresponding to the center region of the Human GJA1 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage Buffer | PBS |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2912240 |
Target Information
Connexin 43 (Cx43) is a member of the gap junction protein family. Connexins assemble as hexamers and are transported to the plasma membrane to create hemichannels that can associate with hemichannels on nearby cells to form cell-to-cell channels. Clusters of these channels assemble to make gap junctions, which are important in development and regulation of cell growth.
Phosphorylation of Cx43 regulates assembly and function of gap junctions. Ser368 of Cx43 is phosphorylated by protein kinase C (PKC) after activation by phorbol esters, decreasing cell-to-cell communication. Src can interact with and phosphorylate Cx43 to alter gap junction communication. GFAP are membrane-spanning proteins that facilitate the transfer of ions and small molecules between cells.
Based on sequence similarities, gap junction proteins are divided into alpha and beta categories. Connexin 43 is the major protein of gap junctions in the heart and plays a crucial role in synchronized cardiac contraction and embryonic development. Connexin 43 is also targeted by several protein kinases that regulate myocardial cell-cell coupling. A related intron-less pseudogene, GJA1P, has been mapped to chromosome 5. Mutations in the GFAP gene cause X-linked Charcot-Marie-Tooth disease, oculodentodigital dysplasia, and heart malformations. Alternatively spliced transcript variants of GFAP have been found.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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