SHFM1 (Human) Recombinant Protein (P01)
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Specification
Product Description
Human SHFM1 full-length ORF ( NP_006295.1, 1 a.a. - 70 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MSEKKQPVDLGLLEEDDEFEEFPAEDWAGLDEDEDAHVWEDNWDDDNVEDDFSNQLRAELEKHGYKMETS
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
34.7
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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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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