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Merck

HPA062866

Sigma-Aldrich

Anti-CELSR3 antibody produced in rabbit

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution

别名:

Anti-CDHF11, Anti-EGFL1, Anti-FMI1, Anti-HFMI1, Anti-MEGF2

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About This Item

分類程式碼代碼:
12352203
人類蛋白質圖譜編號:
NACRES:
NA.43

生物源

rabbit

品質等級

共軛

unconjugated

抗體表格

affinity isolated antibody

抗體產品種類

primary antibodies

無性繁殖

polyclonal

產品線

Prestige Antibodies® Powered by Atlas Antibodies

形狀

buffered aqueous glycerol solution

物種活性

human

技術

immunohistochemistry: 1:2500-1:5000

免疫原序列

LDSLSRSSNSREQLDQVPSRHPSREALGPLPQLLRAREDSVSGPSHGPSTEQLDILSSILASFNSSALSSVQSSSTP

UniProt登錄號

運輸包裝

wet ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... CELSR3(1951)

一般說明

Cadherin EGF LAG seven-pass G-type receptor 3 (CELSR3) is also called multiple epidermal growth factor (EGF)-like domains protein 2 (MEGF2). It has transmembrane regions, six EGF-like domains, eight cadherin motifs and two laminin G domains. The MEGF2 is mapped to human chromosome 3p21.31.

免疫原

cadherin, EGF LAG seven-pass G-type receptor 3

應用

All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry.

The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. We also provide Prestige Antibodies® protocols and other useful information.

生化/生理作用

Cadherin EGF LAG seven-pass G-type receptor 3 (CELSR3) is critical for development of axon and nerve cell polarity. Microdeletion in the CELSR3 gene locus leads to developmental delay and facial dysmorphism. Polymorphisms in CELSR3 and frizzled (FZD) contributes to congenital disorder, hirschsprung disease. Hypermethylation of CELSR3 is implicated in progression of oral carcinoma.

特點和優勢

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

聯結

Corresponding Antigen APREST87998

外觀

Solution in phosphate buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide.

法律資訊

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

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 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析证书(COA)

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访问文档库

Identification of high-molecular-weight proteins with multiple EGF-like motifs by motif-trap screening
Nakayama M, et al.
Genomics, 51(1), 27-34 (1998)
A 3.1-Mb microdeletion of 3p21. 31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay
Haldeman-Englert CR, et al.
European Journal of Medical Genetics, 52(4), 265-268 (2009)
Celsr3 and Fzd3 in axon guidance
Chai G, et al.
The International Journal of Biochemistry & Cell Biology, 64(4), 11-14 (2015)
Protocadherin Celsr3 is crucial in axonal tract development
Tissir F, et al.
Nature Neuroscience, 8(4), 451-457 (2005)
Involvement of CELSR3 hypermethylation in primary oral squamous cell carcinoma
Khor GH, et al.
Asian Pacific Journal of Cancer Prevention, 17(1), 219-223 (2016)

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