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Rabbit Anti-FAM70A  antibody (bs-11006R)  
~~~促銷代碼KT202411~~~
訂購(gòu)熱線:400-901-9800
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說(shuō)明書: 50ul  100ul  200ul
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-11006R
英文名稱 Rabbit Anti-FAM70A  antibody
中文名稱 FAM70A蛋白抗體
別    名 family with sequence similarity 70, member A; FLJ20716; hypothetical protein T255A_HUMAN.  
Specific References  (1)     |     bs-11006R has been referenced in 1 publications.
[IF=5.753] Zhang NN et al. Fam70A binds Wnt5a to regulate meiosis and quality of Mouseoocytes. Cell Prolif. 2020 Jun;53(6):e12825.  WB IHC IF IP ;  Mouse.  
研究領(lǐng)域 細(xì)胞生物  發(fā)育生物學(xué)  染色質(zhì)和核信號(hào)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human,Mouse,Rabbit,Sheep,Dog,Horse)
產(chǎn)品應(yīng)用 WB=1:500-2000,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 38kDa
細(xì)胞定位 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FAM70A: 1-100/394 
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 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. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. 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. The FAM70A gene product has been provisionally designated FAM70A pending further characterization.

Subcellular Location:
Membrane; Multi-pass membrane protein

Similarity:
Belongs to the TMEM255 family.

SWISS:
Q5JRV8

Gene ID:
55026

Database links:

Entrez Gene: 55026 Human

Entrez Gene: 245386 Mouse

Entrez Gene: 313453 Rat

SwissProt: Q9BE63 Cynomolgus monkey

SwissProt: Q5JRV8 Human

SwissProt: Q8BHW5 Mouse

SwissProt: Q7TMP6 Rat

Unigene: 437563 Human

Unigene: 72979 Mouse

Unigene: 163441 Rat



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