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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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Phospho-Connexin 43 (Ser368) Rabbit Polyclonal Antibody로, 인간·마우스·랫트 시료에 반응합니다. Western blot, IHC, ICC에 적합하며, 항원 친화 크로마토그래피로 정제되었습니다. 세포막 및 세포접합부에서 Connexin 43 인산화 연구에 유용합니다.

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마지막 업데이트 2025. 08. 04. 오후 07:36
Thermo Fisher Scientific 602-960 Phospho-Connexin 43 (Ser368) Polyclonal Antibody 100 ug pk판매 단위 pk ·
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423,300원VAT 포함 465,630원

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

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 0.1–1 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 2–10 µg/mL
Immunocytochemistry (ICC/IF) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to the C-terminal region of human Connexin 43 with phosphorylated Ser368
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Antigen affinity chromatography
Storage Buffer 25 mM Tris with proprietary stabilizer
Contains 0.01% Sodium azide
Storage Conditions Store at 4°C short term. For long term, store at -20°C. Avoid freeze/thaw cycles.

Product Specific Information

  • Positive control: Human cardiac muscle
  • Cellular location: Cell membrane, Cell junction

Target Information

Connexin 43 (Cx43) belongs to the gap junction protein family. Connexins assemble as hexamers forming hemichannels that connect adjacent cells, enabling intercellular communication. Phosphorylation of Cx43, particularly at Ser368 by protein kinase C (PKC), regulates the assembly and function of gap junctions by decreasing cell-to-cell communication.

Cx43 is the predominant gap junction protein in cardiac tissue, playing a crucial role in synchronized heart contraction and embryonic development. It is also regulated by various kinases affecting myocardial cell coupling. A related pseudogene, GJA1P, is located on chromosome 5.

Mutations in related genes can lead to disorders such as 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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