Emerin/EMD Rabbit mAb (AMR12399N)

• Background:

  Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene. [provided by RefSeq, Jul 2008]

• Synonyms:

  EDMD; LEMD5; STA

• Gene ID:

  2010

• UniProt:

  P50402

• Cellular Locus:

  Nucleoplasmic side, Nucleus inner membrane, Nucleus outer membrane, Single-pass membrane protein

• Dilution:

  WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200

• Form:

  Liquid

• Buffer:

  Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3.

• Molecular Weight:

  Calculated MW: 29kDa Observed MW: 30KDa/35KDa

• Storage Conditions:

  Store at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

• Overview:

  We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality Emerin/EMD Rabbit mAb (AMR12399N) .

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=2010

• Uniprot URL:

  https://www.uniprot.org/uniprot/P50402

• AA Sequence:

  Email for sequence