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重要文件

C6344

Sigma-Aldrich

Monoclonal Anti-Connexin-32 antibody produced in mouse

clone CXN-32, ascites fluid, buffered aqueous solution

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About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.41
共軛:
unconjugated
application:
ARR
ELISA (i)
IHC (f)
WB
無性繁殖:
CXN-32, monoclonal
物種活性:
human, rat, mouse
citations:
10
技術:
immunohistochemistry (frozen sections): suitable
indirect ELISA: suitable
microarray: suitable
western blot: 1:1,000 using a mouse whole brain extract
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生物源

mouse

品質等級

共軛

unconjugated

抗體表格

ascites fluid

抗體產品種類

primary antibodies

無性繁殖

CXN-32, monoclonal

形狀

buffered aqueous solution

分子量

antigen 27 kDa

包含

15 mM sodium azide

物種活性

human, rat, mouse

技術

immunohistochemistry (frozen sections): suitable
indirect ELISA: suitable
microarray: suitable
western blot: 1:1,000 using a mouse whole brain extract

同型

IgG1

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

一般說明

Monoclonal Anti-Connexin-32 (mouse IgG1 isotype) is derived from the CXN-32 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse. The 27 kDa connexin protein (Connexin-32, Cx32), belongs to the connexion family of proteins. It is expressed in most tissues, even though the pattern of expression may differ in various cell types including peripheral and central nervous system.

免疫原

synthetic connexin-32 peptide (amino acids 105-123).

應用

Monoclonal Anti-Connexin-32 antibody produced in mouse has been used in:
  • enzyme linked immunosorbent assay (ELISA)
  • immunoblotting
  • epifuorescent microscopy

生化/生理作用

Connexin-32 low expression levels is observed in common bile duct ligation (CBDL). In addition, a combination of myelin disruption and axonal degeneration has been shown to occur with Cx32 mutations in Charcot-Marie-Tooth disease (CMTX). Monoclonal antibodies reacting specifically with Cx32, may be used in diverse cellular and molecular approaches to the study of gap junctions and their properties, and to correlate their expression pattern with physiological functions or pathological conditions.
Connexins belong to the gap junction protein family. In humans, connexin is encoded by GJB1 (gap junction protein, β 1) gene. The gap junction proteins connexin32 (Cx32), Cx37, Cx40 and Cx43 are expressed in endothelial cells and regulate vascular functions involving inflammation. The endothelial Cx32 positively regulates angiogenesis by enhancing endothelial cell tube formation and cell migration. CX32 mutation is associated with cognitive impairment and a differential degree of peripheral nerve involvement.

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), 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

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Connexins modulate autophagosome biogenesis
Bejarano E, et al.
Nature Cell Biology, 16(5), 401-401 (2014)
Three-dimensional binding of epidermal growth factor peptides in colonic tissues produced from rotating bioreactor
Kaeffer B, et al.
In Vitro Cellular & Developmental Biology. Animal, 38(8), 436-439 (2002)
Takayuki Okamoto et al.
Experimental cell research, 321(2), 133-141 (2013-12-18)
The gap junction proteins connexin32 (Cx32), Cx37, Cx40, and Cx43 are expressed in endothelial cells, and regulate vascular functions involving inflammation, vasculogenesis and vascular remodeling. Aberrant Cxs expression promotes the development of atherosclerosis which is modulated by angiogenesis; however the
Role of the p38 MAP-kinase signaling pathway for Cx32 and claudin-1 in the rat liver
Kojima T, et al.
Cell communication & adhesion, 10(4-6), 437-443 (2003)
What?s the function of connexin 32 in the peripheral nervous system?
Bortolozzi M
Frontiers in Molecular Neuroscience, 11 (2018)

文章

Cancer research has revealed that the classical model of carcinogenesis, a three step process consisting of initiation, promotion, and progression, is not complete.

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