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FUNDC2 Rabbit pAb (bs-16195R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-16195R
英文名稱 FUNDC2 Rabbit pAb
中文名稱 Cervical cancer oncogene 3/宮頸癌原癌基因3抗體
別    名 Cervical cancer oncogene 3; Cervical cancer proto oncogene 3 protein; DC44; FLJ33773; FUN14 domain containing 2; FUN14 domain containing protein 2; FUNDC 2; HCBP 6; HCBP6; FUND2_HUMAN; HCC 3; HCC3; Hepatitis C virus core binding protein 6; MGC131676; MGC2495; OTTHUMP00000015441; OTTHUMP00000061459; PD03104.  
研究領(lǐng)域 腫瘤  細(xì)胞生物  轉(zhuǎn)錄調(diào)節(jié)因子  細(xì)菌及病毒  新陳代謝  線粒體  表觀遺傳學(xué)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
克 隆 號(hào)
交叉反應(yīng) (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Dog,Horse)
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 21 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞核 細(xì)胞漿 線粒體
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FUNDC2: 101-189/189 
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(xiàng) 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 FUNDC2 is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Function:
The function of FUNDC2 (FUN14 domain-containing protein 2) is unknown.

Subcellular Location:
Mitochondrial

Similarity:
Belongs to the FUN14 family.

SWISS:
Q9BWH2

Gene ID:
65991

Database links:

Entrez Gene: 65991 Human

Entrez Gene: 67391 Mouse

SwissProt: Q9BWH2 Human

SwissProt: Q9D6K8 Mouse

Unigene: 356050 Human

Unigene: 126404 Mouse



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