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Emd (NM_007927) Mouse Recombinant Protein

Product Specifications

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]

Overview

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

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

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

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