KBTBD10 (KLHL41) (NM_006063) Human Recombinant Protein
Product Specifications
Background
This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]
Synonyms
KBTBD10; Krp1; SARCOSIN
Gene ID
10324
UniProt
O60662
Accession Number mRNA
NM_006063
Chromosomal Location
2q31.1
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
67.9 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
KLHL41
Species
Human
Protein ID
NP_006054
Overview
Recombinant protein of human kelch repeat and BTB (POZ) domain containing 10 (KBTBD10)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/10324
Uniprot URL
https://www.uniprot.org/uniprot/O60662
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_006063
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_006054
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