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Rabbit Anti-TMEM176A/AP Conjugated antibody
Rabbit Anti-TMEM176A/AP Conjugated antibody
GS188; HCA112; Hepatocellular carcinoma-associated antigen 112; likley ortholog of mouse GS188; T176A_RAT; Tmem176a; Transmembrane protein 176A.
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  • NO.:SL13623R-AP
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Mouse,Rat,)
    Applications:WB IHC-P IHC-F ICC
    concentration:1mg/ml
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Product Name Anti-TMEM176A/AP
Chinese Name 碱性磷酸酶(AP)标记的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=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 26kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from rat TMEM176A
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage 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.
Product Detail background:
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.

Database links:
 

UniProtKB/Swiss-Prot: Q4G068.1



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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