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Rabbit Anti-TEX261/Biotin Conjugated antibody (bs-12105R-Bio)
訂購(gòu)熱線(xiàn):400-901-9800
訂購(gòu)郵箱:sales@m.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bs-12105R-Bio
英文名稱(chēng)1 Rabbit Anti-TEX261/Biotin Conjugated antibody
中文名稱(chēng) 生物素標(biāo)記的TEX261蛋白抗體
別    名 3110001O07Rik; AA409339; AI480706; AL033351; Protein TEX261; TEG 261; TEX261; TX261_HUMAN; UNQ1882/PRO4325.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢(xún)價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 細(xì)胞生物  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞凋亡  通道蛋白  細(xì)胞膜受體  
抗體來(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng) (predicted: Human, Dog, Pig, Cow, Rabbit, Sheep, )
產(chǎn)品應(yīng)用 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 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 23kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TEX261
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 癈 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癈. 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 癈.
產(chǎn)品介紹 background:
TEX261 is a 196 amino acid multi-pass membrane protein that belongs to the SVP26 family. The gene that encodes TEX261 consists of approximately 47,406 bases and maps to human chromosome 2p13.3. Consisting of 237 million bases, Chromosome 2 encodes over 1,400 genes and makes up approximately 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.

Subcellular Location:
Membrane; Multi-pass membrane protein (Potential).

Similarity:
Belongs to the SVP26 family.

Database links:

Entrez Gene: 113419 Human

Entrez Gene: 21766 Mouse

SwissProt: Q6UWH6 Human

SwissProt: Q62302 Mouse

Unigene: 516087 Human

Unigene: 391476 Mouse



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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