Class A basic helix loop helix protein 9 (BHLHA9) (NM_001164405) Human Recombinant Protein
Product Specifications
Background
This gene is a member of the basic helix-loop-helix family. The encoded protein is a transcription factor involved in limb development. Mutations in this gene have been associated with mesoaxial synostotic syndactyly Malik-Percin type (MSSD) . Copy number variation of a locus containing this gene has been linked to a form of split-hand/foot malformation with long bone deficiency (SHFLD3) . [provided by RefSeq, Mar 2015]
Synonyms
BHLHF42; CCSPD
Gene ID
727857
UniProt
Q7RTU4
Accession Number mRNA
NM_001164405
Chromosomal Location
17p13.3
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Molecular Weight
24 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
BHLHA9
Species
Human
Protein ID
NP_001157877
Overview
Purified recombinant protein of Homo sapiens basic helix-loop-helix family, member a9 (BHLHA9) .
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/727857
Uniprot URL
https://www.uniprot.org/uniprot/Q7RTU4
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001164405
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001157877
Curated Selection
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