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精子發(fā)生相關(guān)蛋白2樣蛋白抗體

參   考   價: 11

訂  貨  量: ≥1 

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產(chǎn)品型號

品       牌Abcam

廠商性質(zhì)生產(chǎn)商

所  在  地上海

更新時間:2015-06-12 09:12:00瀏覽次數(shù):211次

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精子發(fā)生相關(guān)蛋白2樣蛋白抗體
WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù))
not yet tested in other applications.

精子發(fā)生相關(guān)蛋白2樣蛋白抗體

英文名稱 SPATA2L
中文名稱 精子發(fā)生相關(guān)蛋白2樣蛋白抗體
別    名 C16orf76; chromosome 16 open reading frame 76; MGC26885; SPA2L_HUMAN; SPATA2 like protein; SPATA2-like protein; Spata2L; spermatogenesis associated 2 like; Spermatogenesis associated protein 2 like protein; Spermatogenesis-associated protein 2-like protein; tamo.

說 明 書 0.2ml  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse, Rat, Pig, Rabbit, Guinea Pig, 
產(chǎn)品應(yīng)用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù)) 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 46kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human SPATA2L
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.

PubMed PubMed
產(chǎn)品介紹 background:
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximay 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial omeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The gene encoding SPATS2L maps to human locus 2q33.1.

Similarity:
Belongs to the SPATA2 family.

Database links:

Entrez Gene: 124044 Human

Entrez Gene: 498963 Rat

SwissProt: Q8IUW3 Human

Unigene: 374556 Human

Unigene: 91547 Rat



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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