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Rabbit Anti-COTL1  antibody (bs-14002R)  
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產(chǎn)品編號 bs-14002R
英文名稱 Rabbit Anti-COTL1  antibody
中文名稱 肌動蛋白輔助蛋白類樣蛋白抗體
別    名 CLP; Coactosin like 1; Coactosin-like protein; COTL1; COTL1_HUMAN; FLJ43657; MGC19733.  
研究領(lǐng)域 細胞生物  信號轉(zhuǎn)導(dǎo)  結(jié)合蛋白  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Horse)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 16kDa
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human COTL1: 41-142/142 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 This gene encodes one of the numerous actin-binding proteins which regulate the actin cytoskeleton. This protein binds F-actin, and also interacts with 5-lipoxygenase, which is the first committed enzyme in leukotriene biosynthesis. Although this gene has been reported to map to chromosome 17 in the Smith-Magenis syndrome region, the best alignments for this gene are to chromosome 16. The Smith-Magenis syndrome region is the site of two related pseudogenes. [provided by RefSeq, Jul 2008]

Function:
Binds to F-actin in a calcium-independent manner. Has no direct effect on actin depolymerization.

Subcellular Location:
Cytoplasm > cytoskeleton.

Tissue Specificity:
Widely expressed with highest levels in placenta, lung, kidney and peripheral blood leukocytes and lower levels in brain, liver and pancreas.

Similarity:
Belongs to the actin-binding proteins ADF family. Coactosin subfamily.
Contains 1 ADF-H domain.

SWISS:
Q14019

Gene ID:
23406

Database links:

Entrez Gene: 23406 Human

Omim: 606748 Human

SwissProt: Q14019 Human

Unigene: 289092 Human



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