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Rabbit Anti-TEX261 antibody
Rabbit Anti-TEX261 antibody
3110001O07Rik; AA409339; AI480706; AL033351; Protein TEX261; TEG 261; TEX261; TX261_HUMAN; UNQ1882/PRO4325.
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  • NO.:SL12105R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Dog,Pig,Cow,Rabbit,Sheep,)
    Applications:ELISA
    concentration:1mg/ml
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Product Name TEX261
Chinese Name TEX261蛋白抗体
Alias 3110001O07Rik; AA409339; AI480706; AL033351; Protein TEX261; TEG 261; TEX261; TX261_HUMAN; UNQ1882/PRO4325.  
Research Area Cell biology  Neurobiology  Signal transduction  Apoptosis  Channel protein  The cell membrane受体  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Dog, Pig, Cow, Rabbit, Sheep, )
Applications ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 23kDa
Cellular localization The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human TEX261: 121-196/196 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail 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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