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AV34891

Sigma-Aldrich

Anti-ZNF57 antibody produced in rabbit

affinity isolated antibody

同義詞:

Anti-ZNF424, Anti-Zinc finger protein 57

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.41

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

形狀

buffered aqueous solution

分子量

64 kDa

物種活性

human

濃度

0.5 mg - 1 mg/mL

技術

western blot: suitable

NCBI登錄號

UniProt登錄號

運輸包裝

wet ice

儲存溫度

−20°C

基因資訊

human ... ZNF57(126295)

一般說明

ZNF57 codes for a zinc finger protein. Genetic variations in ZNF57 may be a potential cause for Mendelian diseases such as hereditary deafness.
Rabbit Anti-ZNF57 antibody recognizes human ZNF57.

免疫原

Synthetic peptide directed towards the N terminal region of human ZNF57

應用

Rabbit Anti-ZNF57 antibody is suitable for western blot applications at a concentration of 1 μg/ml.

生化/生理作用

ZNF57 belongs to the krueppel C2H2-type zinc-finger protein family. It contains 13 C2H2-type zinc fingers and 1 KRAB domain. ZNF57 may be involved in transcriptional regulation.

序列

Synthetic peptide located within the following region: FTLEEWALLDSAQRDLYRDVMLETFRNLASVDDGTQFKANGSVSLQDMYG

外觀

Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

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 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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存取文件庫

Asli Sirmaci et al.
PloS one, 7(2), e32000-e32000 (2012-03-01)
Whole exome sequencing provides unprecedented opportunities to identify causative DNA variants in rare Mendelian disorders. Finding the responsible mutation via traditional methods in families with hearing loss is difficult due to a high degree of genetic heterogeneity. In this study

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