KBTBD10 (KLHL41) (NM_006063) Human Recombinant Protein

• 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