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Rabbit Anti-TEX261  antibody (bs-12105R)  
~~~促銷代碼KT202411~~~
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說明書: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
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產品編號 bs-12105R
英文名稱 Rabbit Anti-TEX261  antibody
中文名稱 TEX261蛋白抗體
別    名 3110001O07Rik; AA409339; AI480706; AL033351; Protein TEX261; TEG 261; TEX261; TX261_HUMAN; UNQ1882/PRO4325.  
研究領域 細胞生物  神經生物學  信號轉導  細胞凋亡  通道蛋白  細胞膜受體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Rabbit,Pig,Sheep,Cow,Dog)
產品應用 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 23kDa
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TEX261: 121-196/196 
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 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 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.

SWISS:
Q6UWH6

Gene ID:
113419

Database links:

Entrez Gene: 113419 Human

Entrez Gene: 21766 Mouse

SwissProt: Q6UWH6 Human

SwissProt: Q62302 Mouse

Unigene: 516087 Human

Unigene: 391476 Mouse



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