FAM55D蛋白抗体

Quantity size:

0.2ml

Concentration:

1mg/ml FAM55D蛋白抗体  Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

Background:

FAM55D is a 544 amino acid secreted protein that is expressed as two isoforms due to alternative splicing events. The gene encoding FAM55D is located on chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. FAM55D蛋白抗体 The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell FAM55D蛋白抗体 and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM55D gene product has been provisionally designated FAM55D pending further characterization.

 FAM55D蛋白抗体Also known as:

C11orf33; Chromosome 11 open reading frame 33; FA55D_HUMAN; Fam55d; Family with sequence similarity 55 member D; Family with sequence similarity 55, member D; FLJ20127; Hypothetical protein LOC54827; Protein FAM55D.

Specificity:

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Rabbit Polyclonal IgG, affinity purified by Protein A.

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Reacts with: Human, Mouse, Rat, .

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Immunogen: KLH conjugated synthetic peptide derived from human FAM55D.

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 FAM55D蛋白抗体Predicted Molecular Weight: 59kDa.

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  IF=1:100-500   
Not yet tested in other applications. 
Optimal working dilutions must be determined by the end user.

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