WBSCR16 purified MaxPab mouse polyclonal antibody (B01P)
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More Files
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Specification
Product Description
Mouse polyclonal antibody raised against a full-length human WBSCR16 protein.
Immunogen
WBSCR16 (AAH07823.1, 1 a.a. ~ 464 a.a) full-length human protein.
Sequence
MALVALVAGARLGRRLSGPGLGRGHWTAAGRSRSRREAAEAEAEVPVVQYVGERAARADRVFVWGFSFSGALGVPSFVVPSSGPGPRAGARPRRRIQPVPYRLELDQKISSAACGYGFTLLSSKTADVTKVWGMGLNKDSQLGFHRSRKDKTRGYEYVLEPSPVSLPLDRPQETRVLQVSCGRAHSLVLTDREGVFSMGNNSYGQCGRKVVENEIYSESHRVHRMQDFDGQVVQVACGQDHSLFLTDKGEVYSCGWGADGQTGLGHYNITSSPTKLGGDLAGVNVIQVATYGDCCLAVSADGGLFGWGNSEYLQLASVTDSTQVNVPRCLHFSGVGKVRQAACGGTGCAVLNGEGHVFVWGYGILGKGPNLVESAVPEMIPPTLFGLTEFNPEIQVSRIRCGLSHFAALTNKGELFVWGKNIRGCLGIGRLEDQYFPWRVTMPGEPVDVACGVDHMVTLAKSFI
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (91); Rat (90)
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)
Western Blot analysis of WBSCR16 expression in transfected 293T cell line (H00081554-T02) by WBSCR16 MaxPab polyclonal antibody.
Lane 1: WBSCR16 transfected lysate(51.04 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — WBSCR16
Entrez GeneID
81554GeneBank Accession#
BC007823Protein Accession#
AAH07823.1Gene Name
WBSCR16
Gene Alias
DKFZp434D0421, MGC189739, MGC44931
Gene Description
Williams-Beuren syndrome chromosome region 16
Gene Ontology
HyperlinkGene Summary
This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq
Other Designations
RCC1-like G exchanging factor-like
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