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Rabbit Anti-TMEM176A antibody
Rabbit Anti-TMEM176A antibody
GS188; HCA112; Hepatocellular carcinoma-associated antigen 112; likley ortholog of mouse GS188; T176A_RAT; Tmem176a; Transmembrane protein 176A.
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Details

Product Name TMEM176A
Chinese Name Transmembrane protein176A抗体
Alias GS188; HCA112; Hepatocellular carcinoma-associated antigen 112; likley ortholog of mouse GS188; T176A_RAT; Tmem176a; Transmembrane protein 176A.  
Research Area Cell biology  Neurobiology  Signal transduction  Stem cells  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Mouse, Rat, )
Applications WB=1:500-2000 ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 26kDa
Cellular localization The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from rat TMEM176A: 21-120/245 
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 TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

Subcellular Location:
Membrane.

Similarity:
Belongs to the TMEM176 family.

SWISS:
Q4G068

Gene ID:
297077

Database links:

Entrez Gene: 55365 Human

Entrez Gene: 66058 Mouse

Entrez Gene: 297077 Rat

Omim: 610334 Human

SwissProt: Q96HP8 Human

SwissProt: Q9DCS1 Mouse

SwissProt: Q4G068 Rat

Unigene: 647116 Human

Unigene: 27061 Mouse

Unigene: 17071 Rat



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