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Thermo Fisher Scientific Phospho-Connexin 43 (Tyr265) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-Connexin 43 (Tyr265) Polyclonal Antibody

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Human Connexin 43의 Tyr265 인산화 부위를 인식하는 Rabbit Polyclonal Antibody. Western blot에 적합하며, HUVEC 세포에서 양성 대조군으로 사용 가능. Affinity chromatography로 정제된 액상 형태, -20°C 보관.

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마지막 업데이트 2025. 07. 24. 오후 03:42
Thermo Fisher Scientific PA537584 Phospho-Connexin 43 (Tyr265) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-Connexin 43 (Tyr265) Polyclonal Antibody

Applications

Western Blot (WB)


Product Specifications

항목 내용
Species Reactivity Human
Published Species Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Peptide sequence around phosphorylation site of Tyrosine 265 (Q-K-Y(p)-A-Y) derived from Human Connexin 43
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity 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_2554192

Product Specific Information

Connexin 43 antibody detects endogenous levels of Connexin 43 only when phosphorylated at Tyrosine 265.
A suggested positive control for Western blot is HUVEC cells.


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 connect adjacent cells, forming gap junctions. These junctions are essential for cell growth regulation and development.

Phosphorylation of Cx43 regulates gap junction assembly and function. Ser368 of Cx43 is phosphorylated by PKC following activation by phorbol esters, reducing intercellular communication. Src kinase can also phosphorylate Cx43, modulating gap junction activity.

Connexin 43 is the major gap junction protein in the heart, playing a key role in synchronized cardiac contraction and embryonic development. A related pseudogene, GJA1P, is located on chromosome 5. Mutations in the GFAP gene are associated with X-linked Charcot-Marie-Tooth disease, oculodentodigital dysplasia, and heart malformations.


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

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