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Rabbit Anti-FAM50B antibody
Rabbit Anti-FAM50B antibody
D0H6S2654E; D6S2654E; DNA segment, human D6S2654E; FA50B_HUMAN; FAM50B; Family with sequence similarity 50, member B; Protein FAM50B; Protein XAP 5 like; Protein XAP-5-like; X5L.
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Details

Product Name FAM50B
Chinese Name FAM50B蛋白抗体
Alias D0H6S2654E; D6S2654E; DNA segment, human D6S2654E; FA50B_HUMAN; FAM50B; Family with sequence similarity 50, member B; Protein FAM50B; Protein XAP 5 like; Protein XAP-5-like; X5L.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Mouse, Rat, Horse, )
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 39kDa
Cellular localization The nucleus Extracellular matrix Secretory protein 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FAM50B: 231-325/325 
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 Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The FAM50B gene product has been provisionally designated FAM50B pending further characterization.

Tissue Specificity:
Widely expressed. Mostly abundant in testis and adult and fetal brain.

Similarity:
Belongs to the FAM50 family.

SWISS:
Q9Y247

Gene ID:
26240

Database links:

Entrez Gene: 26240 Human

SwissProt: Q9Y247 Human

Unigene: 140944 Human



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