WBSCR22 purified MaxPab rabbit polyclonal antibody (D01P)
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human WBSCR22 protein.
Immunogen
WBSCR22 (NP_059998.2, 1 a.a. ~ 281 a.a) full-length human protein.
Sequence
MASRGRRPEHGGPPELFYDETEARKYVRNSRMIDIQTRMAGRALELLYLPENKPCYLLDIGCGTGLSGSYLSDEGHYWVGLDISPAMLDEAVDREIEGDLLLGDMGQGIPFKPGTFDGCISISAVQWLCNANKKSENPAKRLYCFFASLFSVLVRGSRAVLQLYPENSEQLELITTQATKAGFSGGMVVDYPNSAKAKKFYLCLFSGPSTFIPEGLSENQDEVEPRESVFTNERFPLRMSRRGMVRKSRAWVLEKKERHRRQGREVRPDTQYTGRKRKPRF
Host
Rabbit
Reactivity
Human, Mouse, Rat
Interspecies Antigen Sequence
Mouse (79); Rat (79)
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 (Tissue lysate)
WBSCR22 MaxPab rabbit polyclonal antibody. Western Blot analysis of WBSCR22 expression in mouse testis.Western Blot (Tissue lysate)
WBSCR22 MaxPab rabbit polyclonal antibody. Western Blot analysis of WBSCR22 expression in rat brain.Western Blot (Cell lysate)
WBSCR22 MaxPab rabbit polyclonal antibody. Western Blot analysis of WBSCR22 expression in Hela S3 NE.Western Blot (Transfected lysate)
Western Blot analysis of WBSCR22 expression in transfected 293T cell line (H00114049-T02) by WBSCR22 MaxPab polyclonal antibody.
Lane 1: WBSCR22 transfected lysate(31.90 KDa).
Lane 2: Non-transfected lysate.
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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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