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Merck

SAB4200819

Sigma-Aldrich

Anti-Connexin 43 antibody, Mouse monoclonal

clone CXN-6, purified from hybridoma cell culture

别名:

Cx43, Gap junction 43 kDa heart protein, Gap junction alpha-1 protein

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

mouse

抗體表格

purified from hybridoma cell culture

抗體產品種類

primary antibodies

無性繁殖

CXN-6, monoclonal

分子量

~43 kDa

物種活性

porcine, feline, chicken, mouse, human, rat

包裝

antibody small pack of 25 μL

濃度

~1 mg/mL

技術

immunoblotting: 0.5-1 μg/mL
immunofluorescence: 10-20 μg/mL

同型

IgM

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

Porcine ... GJA1(100518636)
chicken ... GJA1(395278)
feline ... GJA1(101100211)
human ... GJA1(2697)
mouse ... GJA1(14609)
rat ... GJA1(24392)

一般說明

Monoclonal Anti-Connexin 43 (mouse IgM isotype) is derived from the hybridoma CXN-6 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide from the C-terminal region of Connexin 43 protein, conjugated to KLH. Connexin 43 protein (Cx43), also known as Gap junction α-1 protein or Gap junction 43 kDa heart protein. It has four transmembrane domains (TMs). The N and C-terminal cytoplasmic tails orient in plasma membrane. It also has two extracellular loop (EL) domains and a cytoplasmic loop (CL). Six connexin subunits form a connexon or hemichannel in the plasma membrane and a head-to-head docking between two hemichannels result in the formation of a gap junction channel. Cx43 is expressed in heart and brain. It is expressed in cell types including the melanocytes, keratinocytes, endothelial and basal cells. Cx43 has been mapped to human chromosome 6q22.31.

特異性

Monoclonal Anti-Connexin 43 specifically recognizes Connexin 43 from human1,2, mouse2, rat3, porcine4, chicken5 and feline6 origin. 

免疫原

Synthetic peptide corresponding to human connexin-43 C-terminal region, conjugated to KLH

應用

The antibody may be used in various immunochemical techniques including Immunoblot (~43 kDa), Immunohistochemistry and Immunofluorescence. 

生化/生理作用

Connexin 43 (Cx43) functions as a neuroprotector and is most prominently expressed in astrocytes and microglial cells in the brain. It plays a key role in intercellular communication. Cx43 mediates synchronized contraction of the heart. It modulates of the cell migration and cell adhesion processes. Altered connexin 43 expression is implicated in hypertrophic cardiomyopathy. It is less expressed in human tumors. It is a potential target for treating skin disorders. Its downregulation favours wound healing.

外觀

Supplied as a solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide as a preservative.

儲存和穩定性

For continuous use, store at 2-8°C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

免責聲明

Unless otherwise stated in our catalog  our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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访问文档库

Connexin 43: key roles in the skin
Zhang XF and Cui X
Biomedical Reports, 6(6), 605-611 (2017)
Cardiac Cx43, Cx40 and Cx45 co-assembling: involvement of connexins epitopes in formation of hemichannels and Gap junction channels
Desplantez T
BMC Cell Biology, 18(1), 3-3 (2017)
Genetics of vascular malformations
Seminars in Pediatric Surgery, 23(4), 221-226 (2014)
Gap junction-mediated transfer of miR-145-5p from microvascular endothelial cells to colon cancer cells inhibits angiogenesis
Thuringer D, et al.
Testing, 7(19), 28160-28160 (2016)
Role of connexin 43 in cardiovascular diseases
Michela P, et al.
European Journal of Pharmacology, 768, 71-76 (2015)

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