SHFM1 DNAxPab
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human SHFM1 DNA using DNAx™ Immune technology.
Technology
Immunogen
Full-length human DNA
Sequence
MSEKKQPVDLGLLEEDDEFEEFPAEDWAGLDEDEDAHVWEDNWDDDNVEDDFSNQLRAELEKHGYKMETS
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 — SHFM1
Entrez GeneID
7979GeneBank Accession#
NM_006304.1Protein Accession#
NP_006295.1Gene Name
SHFM1
Gene Alias
DSS1, ECD, SEM1, SHFD1, SHSF1, Shfdg1
Gene Description
split hand/foot malformation (ectrodactyly) type 1
Omim ID
183600Gene Ontology
HyperlinkGene Summary
The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq
Other Designations
deleted in split-hand/split-foot 1|split hand/foot malformation type 1
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Interactome
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Pathway
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Disease
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