CLN6 (NM_017882) Human Recombinant Protein
Selected Variant
PH41150M5
Size: 20 µg
Product Specifications
Background
This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL) . Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function. [provided by RefSeq, Oct 2008]
Overview
Recombinant protein of human ceroid-lipofuscinosis, neuronal 6, late infantile, variant (CLN6)
Synonyms
CLN4A; HsT18960; nclf
Gene ID
54982
UniProt
Q9NWW5, A0A024R601
Accession Number mRNA
NM_017882
Chromosomal Location
15q23
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
Function
Transmembrane
Molecular Weight
35.7 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
CLN6
Species
Human
Protein ID
NP_060352
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/54982
Uniprot URL
https://www.uniprot.org/uniprot/Q9NWW5
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_017882
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_060352
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