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Cln3 (NM_001146311) Mouse Recombinant Protein

Product Specifications

Background

This gene encodes a transmembrane protein called battenin that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis genes, cause a number of neurodegenerative diseases collectively known as neuronal ceroid lipofuscinoses, the most common of which is juvenile neuronal ceroid-lipofuscinosis (Batten disease) . Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]

Overview

Purified recombinant protein of Mouse ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease) (Cln3), with C-terminal MYC/DDK tag, expressed in HEK293T cells, 20ug

Synonyms

AI323623; batt

Gene ID

12752

UniProt

Q61124

Accession Number mRNA

NM_001146311

Chromosomal Location

7 69.16 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

47.7 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

Cln3

Species

Mouse

Protein ID

NP_001139783

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/12752

Uniprot URL

https://www.uniprot.org/uniprot/Q61124

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_001146311

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_001139783

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