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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]

Overview

Recombinant protein of human CWF19-like 1, cell cycle control (S. pombe) (CWF19L1)

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

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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