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KIAA1429 Rabbit pAb (bs-17003R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產(chǎn)品編號 bs-17003R
英文名稱 KIAA1429 Rabbit pAb
中文名稱 KIAA1429蛋白抗體
別    名 DKFZp434I116; DKFZp781B2117; fSAP121; KIAA1429; MGC138493; MGC141940; MSTP054; Protein virilizer homolog; VIR_HUMAN.  
研究領(lǐng)域 細(xì)胞生物  信號轉(zhuǎn)導(dǎo)  轉(zhuǎn)錄調(diào)節(jié)因子  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應(yīng) (predicted: Human,Mouse,Rat,Rabbit,Sheep,Cow,Horse,Rhesus monkey,Gorilla, Orangutan,Platypus)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/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 202 kDa
檢測分子量
細(xì)胞定位 細(xì)胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KIAA1429: 1661-1760/1812 
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 Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The KIAA1429 gene product has been provisionally designated KIAA1429 pending further characterization.

Function:
May be involved in mRNA splicing regulation.

Subcellular Location:
Nucleus.

Similarity:
Belongs to the vir family.

SWISS:
Q69YN4

Gene ID:
25962

Database links:

Entrez Gene: 25962 Human

Entrez Gene: 66185 Mouse

SwissProt: Q69YN4 Human

SwissProt: A2AIV2 Mouse

Unigene: 202238 Human



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