TRMT61B蛋白抗体

Quantity size:

0.2ml

Concentration:

1mg/ml TRMT61B蛋白抗体  Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

Background:

The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making 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 associatedTRMT61B蛋白抗体 with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome TRMT61B蛋白抗体2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FLJ20628 gene product has been provisionally designated FLJ20628 pending further characterization.

Also known as:

DKFZp564I2178; FLJ20628; tRNA methyltransferase 61 homolog B (S. cerevisiae); tRNA methyltransferase 61 homolog B.

TRMT61B蛋白抗体Specificity:

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Rabbit Polyclonal IgG, affinity purified by Protein A.

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Reacts with: Human, Cow, Horse, Sheep, .

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Immunogen: KLH conjugated synthetic peptide derived from human TRMT61B.

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Predicted Molecular Weight: 53kDa.

TRMT61B蛋白抗体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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