| 產(chǎn)品編號(hào) | bs-11006R |
| 英文名稱 | FAM70A Rabbit pAb |
| 中文名稱 | FAM70A蛋白抗體 |
| 別 名 | family with sequence similarity 70, member A; FLJ20716; hypothetical protein T255A_HUMAN. |
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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.
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| 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,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 | 38 kDa |
| 檢測(cè)分子量 | |
| 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 SwissProt: Q9BE63 Cynomolgus monkey SwissProt: Q5JRV8 Human SwissProt: Q8BHW5 Mouse Unigene: 437563 Human Unigene: 72979 Mouse Unigene: 163441 Rat |
