7号染色体开放阅读框29抗体

Quantity size:

0.2ml

Concentration:

1mg/ml 7号染色体开放阅读框29抗体  Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

Background:

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 i7号染色体开放阅读框29抗体s 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. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterization.

7号染色体开放阅读框29抗体Also known as:

C7orf29; CG029_HUMAN; Chromosome 7 open reading frame 29; Hypothetical protein LOC113763; Uncharacterized protein C7orf29.

Specificity:

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Rabbit Polyclonal IgG, 7号染色体开放阅读框29抗体affinity purified by Protein A.

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Reacts with: Human, .

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Immunogen: KLH conjugated synthetic peptide derived from human C7ORF29 .

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Predicted Molecular Weight: 26kDa.

7号染色体开放阅读框29抗体Storage:

Shipped at 4℃, Store at -20℃ (Avoid repeated freeze/thaw cycles).

Application:

WB=1:100-500  ELISA=1:500-1000  IHC-P=1:100-500  IHC-F=1:100-500  ICC=1:100-500  IF=1:100-500   
Not yet tested in other applications. 
Optimal working dilutions must be determined by the end user.

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