EMD 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 EMD protein.
Immunogen
EMD (AAH00738, 1 a.a. ~ 254 a.a) full-length human protein.
Sequence
MDNYADLSDTELTTLLRRYNIPHGPVVGSTRRLYEKKIFEYETQRRRLSPPSSSAASSYSFSDLNSTRGDADMYDLPKKEDALLYQSKGYNDDYYEESYFTTRTYGEPESAGPSRAVRQSVTSFPDADAFHHQVHDDDLLSSSEEECKDRERPMYGRDSAYQSITHYRPVSASRSSLDLSYYPTSSSTSFMSSSSSSSSWLTRRAIRPENRAPGAGLGQDRQVPLWGQLLLFLVFVIVLFFIYHFMQAEEGNPF
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (74)
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 (Cell lysate)
EMD MaxPab polyclonal antibody. Western Blot analysis of EMD expression in 293.Western Blot (Cell lysate)
EMD MaxPab polyclonal antibody. Western Blot analysis of EMD expression in MCF-7.Western Blot (Transfected lysate)
Western Blot analysis of EMD expression in transfected 293T cell line (H00002010-T01) by EMD MaxPab polyclonal antibody.
Lane 1: EMD transfected lysate(27.94 KDa).
Lane 2: Non-transfected lysate.
Immunofluorescence
Immunofluorescence of purified MaxPab antibody to EMD on HeLa cell. [antibody concentration 10 ug/ml] -
Gene Info — EMD
Entrez GeneID
2010GeneBank Accession#
BC000738Protein Accession#
AAH00738Gene Name
EMD
Gene Alias
EDMD, LEMD5, STA
Gene Description
emerin
Gene Ontology
HyperlinkGene Summary
Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene. [provided by RefSeq
Other Designations
LEM domain containing 5|OTTHUMP00000031938|OTTHUMP00000061687
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Interactome
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Disease
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