KCNE1L (KCNE5) (NM_012282) Human Mass Spec Standard

Specifications

Product Data
Description	KCNE1L MS Standard C13 and N15-labeled recombinant protein (NP_036414)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC206502
Predicted MW	15 kDa
Protein Sequence	Sequence Link (showhide) >RC206502 protein sequence Red=Cloning site Green=Tags(s) MNCSESQRLRTLLSRLLLELHHRGNASGLGAGPRPSMGMGVVPDPFVGREVTSAKGDDAYLYILLIMIFY ACLAGGLILAYTRSRKLVEAKDEPSQACAEHEWAPGGALTADAEAAAGSQAEGRRQLASEGLPALAQGAE RV TRTRPLEQKLISEEDLAANDILDYKDDDDKV
Tag	C-Myc/DDK
Purity	> 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration	>0.05 µg/µL as determined by microplate BCA method
Labeling Method	Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer	25 mM Tris-HCl, 100 mM glycine, pH 7.3
Reference Data
RefSeq	NP_036414
RefSeq Size	1465
RefSeq ORF	426
Synonyms	KCNE1L
Locus ID	23630
Cytogenetics	Xq23
Summary	This gene encodes a member of a family of single pass transmembrane domain proteins that function as ancillary subunits to voltage-gated potassium channels. Members of this family affect diverse processes in potassium channel regulation, including ion selectivity, voltage dependence, and anterograde recycling from the plasma membrane. Variants of this gene are associated with idiopathic ventricular fibrillation and Brugada syndrome. [provided by RefSeq, Nov 2016]
Protein Families	Druggable Genome, Ion Channels: Other, Transmembrane

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