Product Name	NSUN5P2
Chinese Name	NSUN5P2蛋白抗体
Alias	FLJ11626; MGC129801; MGC15057; NOL1/NOP2/Sun domain family member 5C; NOL1R2; NOP2/Sun domain family, member 5 pseudogene 2; NOP2/Sun domain family, member 5C (pseudogene); NOP2/Sun domain family, member 5C; NSUN5C; Putative methyltransferase NSUN5C; WBSCR20B; WBSCR20C; Williams-Beuren syndrome chromosomal region 20C protein.
Research Area	Cell biology  immunology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted: Human, )
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	34kDa
Cellular localization	The nucleus
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human NSUN5P2: 231-315/315
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	This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. There is extensive alternative splicing at this locus. [provided by RefSeq, Jul 2013] Function: May have S-adenosyl-L-methionine-dependent methyl-transferase activity. Tissue Specificity: Ubiquitous. DISEASE: NSUN5C is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Similarity: Belongs to the class I-like SAM-binding methyltransferase superfamily. RsmB/NOP family. SWISS: Q63ZY6 Gene ID: 260294 Database links: Entrez Gene: 260294 Human SwissProt: Q63ZY6 Human

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