CWF19L1 (NM_018294) Human Recombinant Protein
Product Specifications
Background
This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
Synonyms
C19L1; hDrn1; SCAR17
Gene ID
55280
UniProt
Q69YN2, A0A0S2Z5E9
Accession Number mRNA
NM_018294
Chromosomal Location
10q24.31
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
60.4 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
CWF19L1
Species
Human
Protein ID
NP_060764
Overview
Recombinant protein of human CWF19-like 1, cell cycle control (S. pombe) (CWF19L1)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/55280
Uniprot URL
https://www.uniprot.org/uniprot/Q69YN2
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_018294
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_060764
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