WBSCR22 DNAxPab
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human WBSCR22 DNA using DNAx™ Immune technology.
Technology
Immunogen
Full-length human DNA
Sequence
MASRGRRPEHGGPPELFYDETEARKYVRNSRMIDIQTRMAGRALELLYLPENKPCYLLDIGCGTGLSGSYLSDEGHYWVGLDISPAMLDEAVDREIEGDLLLGDMGQGIPFKPGTFDGCISISAVQWLCNANKKSENPAKRLYCFFASLFSVLVRGSRAVLQLYPENSEQLELITTQATKAGFSGGMVVDYPNSAKAKKFYLCLFSGPSTFIPEGLSENQDEVEPRESVFTNERFPLRMSRRGMVRKSRAWVLEKKERHRRQGREVRPDTQYTGRKRKPRF
Host
Rabbit
Reactivity
Human
Purification
Protein A
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Immunofluorescence (Transfected cell)
Flow Cytometry (Transfected cell)
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Gene Info — WBSCR22
Entrez GeneID
114049GeneBank Accession#
NM_017528.2Protein Accession#
NP_059998.2Gene Name
WBSCR22
Gene Alias
HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
Gene Description
Williams Beuren syndrome chromosome region 22
Gene Ontology
HyperlinkGene Summary
This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq
Other Designations
Williams Beuren syndrome chromosome region 22 protein|Williams-Beuren candidate region putative methyltransferase
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Interactome
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Pathway
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