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Rabbit Anti-FUNDC2/BF488 Conjugated antibody (bs-16195R-BF488)
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-16195R-BF488
英文名稱 Rabbit Anti-FUNDC2/BF488 Conjugated antibody
中文名稱 BF488標記的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.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  轉錄調節(jié)因子  細菌及病毒  新陳代謝  線粒體  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, )
產(chǎn)品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 21kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FUNDC2
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產(chǎn)品介紹 background:
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.

Database links:

Entrez Gene: 65991 Human

Entrez Gene: 67391 Mouse

SwissProt: Q9BWH2 Human

SwissProt: Q9D6K8 Mouse

Unigene: 356050 Human

Unigene: 126404 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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