Emd (NM_007927) Mouse Recombinant Protein

• Background:

  This gene is the founding member of the LEM (Lap2beta, Emerin, and Man1) domain gene family. It encodes an integral membrane protein of the inner nuclear membrane. This gene may be involved in transcriptional regulation and genomic organization. In humans, mutations in this gene cause a class of diseases called laminopathies, which includes Emery-Dreifuss muscular dystrophy (EDMD) . [provided by RefSeq, Apr 2013]

• Synonyms:

  AW550900; Sta

• Gene ID:

  13726

• UniProt:

  O08579, A2AM95

• Accession Number mRNA:

  NM_007927

• Chromosomal Location:

  X 37.92 cM

• 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:

  29.4 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:

  Emd

• Species:

  Mouse

• Protein ID:

  NP_031953

• Overview:

  Purified recombinant protein of Mouse emerin (Emd), with C-terminal MYC/DDK tag, expressed in HEK293T cells, 20ug

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/13726

• Uniprot URL:

  https://www.uniprot.org/uniprot/O08579

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_007927

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_031953