| 產(chǎn)品編號(hào) | bs-17726R-BF555 | 
| 英文名稱 | Rabbit Anti-MOSPD1/BF555 Conjugated antibody | 
| 中文名稱 | BF555標(biāo)記的精子運(yùn)動(dòng)結(jié)構(gòu)域蛋白1抗體 | 
| 別 名 | DJ473B4; MOSPD1; Motile sperm domain containing 1; Motile sperm domain-containing protein 1; MSPD1_HUMAN. | 
| 規(guī)格價(jià)格 | 100ul/2980元 購(gòu)買 大包裝/詢價(jià) | 
| 說(shuō) 明 書(shū) | 100ul | 
| 研究領(lǐng)域 | 細(xì)胞生物 發(fā)育生物學(xué) 細(xì)胞膜蛋白 | 
| 抗體來(lái)源 | Rabbit | 
| 克隆類型 | Polyclonal | 
| 交叉反應(yīng) | (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Rabbit, Zebrafish, Cat, ) | 
| 產(chǎn)品應(yīng)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 | 24kDa | 
| 性 狀 | Lyophilized or Liquid | 
| 濃 度 | 1mg/ml | 
| 免 疫 原 | KLH conjugated synthetic peptide derived from human MOSPD1 | 
| 亞 型 | IgG | 
| 純化方法 | affinity purified by Protein A | 
| 儲(chǔ) 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: MOSPD1 is a 213 amino acid multi-pass membrane protein that contains one MSP domain and exists as three alternatively spliced isoforms. The gene encoding MOSPD1 maps to human chromosome Xq26.3. 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 unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and 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 Subcellular Location: Membrane. Similarity: Contains 1 MSP domain. Database links: Entrez Gene: 56180 Human Entrez Gene: 70380 Mouse Omim: 300674 Human SwissProt: Q9UJG1 Human SwissProt: Q8VEL0 Mouse Unigene: 726077 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.  |