CLN6 Proteine
(Ceroid-Lipofuscinosis, Neuronal 6, Late Infantile, Variant (CLN6))
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].
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CLN6
Spezies: Human
Wirt: Wheat germ
Recombinant
ELISA, WB, AA, AP
1 image
CLN6
Spezies: Human
Wirt: Escherichia coli (E. coli)
Recombinant
ELISA, WB, SDS
custom-made
CLN6
Spezies: Human
Wirt: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
CLN6
Spezies: Human
Wirt: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliase für CLN6 Proteine
ceroid-lipofuscinosis, neuronal 6 (Cln6) ProteineCLN6, transmembrane ER protein (CLN6) Proteine
CLN6, transmembrane ER protein S homeolog (cln6.S) Proteine
ceroid-lipofuscinosis, neuronal 6, late infantile, variant (CLN6) Proteine
CLN6, transmembrane ER protein (Cln6) Proteine
CLN6, transmembrane ER protein a (cln6a) Proteine
1810065L06Rik Proteine
AW743417 Proteine
CLN4A Proteine
cln6 Proteine
D9Bwg1455e Proteine
HsT18960 Proteine
nclf Proteine
zgc:103565 Proteine
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