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GATAD1 Rabbit pAb (bs-11921R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
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產品編號 bs-11921R
英文名稱 GATAD1 Rabbit pAb
中文名稱 眼發育相關基因蛋白ODAG抗體
別    名 ODAG; GATA zinc finger domain containing 1; Ocular development associated gene; GATA zinc finger domain-containing protein 1; ocular development-associated gene protein; GATAD1 protein; ocular development associated; ODAG; RG083M05.2; tcag7.279; GATD1_HUMAN.  
Specific References  (1)     |     bs-11921R has been referenced in 1 publications.
[IF=4.3] Ma, Xiaoling, et al. "Decreased expression and DNA methylation levels of GATAD1 in preeclamptic placentas." Cellular Signalling (2014).  IHC-P ;  Human.  
研究領域 細胞生物  神經生物學  信號轉導  生長因子和激素  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Zebrafish,Chicken,Dog,Horse)
產品應用 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 29 kDa
檢測分子量
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GATAD1/ODAG: 61-160/269 
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
產品介紹 The protein encoded by this gene contains a zinc finger at the N-terminus, and is thought to bind to a histone modification site that regulates gene expression. Mutations in this gene have been associated with autosomal recessive dilated cardiomyopathy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012]

Function:
ODAG (Ocular development-associated gene), a novel transcription factor located on chromosome 7, encodes a protein that may play a role in eye development. mRNA profiling in multiple human tissue indicates that ODAG is expressed in human CD56+ NK cells and thyroid tissue.

Subunit:
Component of a chromatin complex, at least composed of KDM5A, GATAD1 and EMSY.

Subcellular Location:
Nuclear

Tissue Specificity:
Ubiquitously expressed among various tissue types. Expressed in left ventricular myocytes.

DISEASE:
Defects in GATAD1 are the cause of cardiomyopathy, dilated type 2B (CMD2B) [MIM:614672]. CMD2B is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.

Similarity:
Contains 1 GATA-type zinc finger.

SWISS:
Q8WUU5

Gene ID:
57798

Database links:

Entrez Gene: 57798 Human

Entrez Gene: 67210 Mouse

SwissProt: Q8N5Y5 Human

SwissProt: Q8WUU5 Human

SwissProt: Q3TS14 Mouse

SwissProt: Q8VCQ2 Mouse

SwissProt: Q920S3 Mouse

SwissProt: Q9CSG2 Mouse

Unigene: 21145 Human



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