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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

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