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Rabbit Anti-MOSPD1/FITC Conjugated antibody (bs-17726R-FITC)
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-17726R-FITC
英文名稱1 Rabbit Anti-MOSPD1/FITC Conjugated antibody
中文名稱 FITC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 購買        大包裝/詢價(jià)
說 明 書 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

Entrez Gene: 317312 Rat

Omim: 300674 Human

SwissProt: Q9UJG1 Human

SwissProt: Q8VEL0 Mouse

SwissProt: Q5RJS6 Rat

Unigene: 726077 Human



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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