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Thermo Fisher Scientific Phospho-Connexin 43 (Ser368) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-Connexin 43 (Ser368) Polyclonal Antibody

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인간, 마우스, 랫트의 Connexin 43 (Ser368) 인산화 형태를 특이적으로 검출하는 폴리클로날 항체. Western blot, IHC, ICC/IF에 사용 가능. PKC 매개 인산화 연구 및 세포 간 신호전달 조절 연구에 적합. 연구용으로만 사용.

카탈로그번호
PA5104820
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 08:19
Thermo Fisher Scientific PA5104820 Phospho-Connexin 43 (Ser368) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-Connexin 43 (Ser368) Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:100–1:500

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human GJA1 (Accession P17302), corresponding to amino acid residues around phosphorylated Ser368.
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Sequential chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2816293

Product Specific Information

This antibody detects endogenous levels of Connexin 43 (GJA1) only when phosphorylated at Serine 368.

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 form hemichannels that connect adjacent cells, creating cell-to-cell communication pathways known as gap junctions.
Phosphorylation of Cx43, particularly at Ser368 by protein kinase C (PKC) upon phorbol ester activation, modulates gap junction assembly and function by decreasing intercellular communication. Src kinase can also interact with and phosphorylate Cx43, altering junctional communication.

Cx43 is the predominant gap junction protein in the heart, playing a critical role in synchronized cardiac contraction and embryonic development. It is regulated by several kinases that modulate myocardial cell coupling. A related intron-less pseudogene, GJA1P, is mapped to chromosome 5.

Mutations in gap junction-related genes are associated with disorders such as X-linked Charcot-Marie-Tooth disease, oculodentodigital dysplasia, and cardiac malformations.

For Research Use Only. Not for use in diagnostic procedures or resale without authorization.

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