Product Name	TENT5A
Chinese Name	TENT5A蛋白抗体
Alias	C6orf37; Terminal nucleotidyltransferase 5A; Chromosome 6 open reading frame 37; TET5A_HUMAN; FAM46A; Family with sequence similarity 46, member A; FLJ20037; HBV X-transactivated gene 11 protein; HBV XAg-transactivated protein 11; Hypothetical protein LOC55603; Retinal expressed gene C6orf37; RGD1311381; XTP11.
Research Area	Tumour  Cell biology  immunology  Neurobiology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted: Human, Mouse, Rat, Dog, Cow, )
Applications	ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （Paraffin sections need antigen repair） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight	50kDa
Cellular localization	The nucleus cytoplasmic
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human TENT5A: 201-300/442
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 FAM46A gene product has been provisionally designated FAM46A pending further characterization. Tissue Specificity: Widely expressed, with preferential expression observed in the retina compared to other ocular tissues. Similarity: Belongs to the FAM46 family. SWISS: Q96IP4 Gene ID: 55603 Database links: Entrez Gene: 55603 Human Entrez Gene: 212943 Mouse Omim: 611357 Human SwissProt: Q96IP4 Human Unigene: 10784 Human

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