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]
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
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
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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