CLN6 蛋白
(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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5 results :
custom-made
CLN6
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
custom-made
CLN6
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
CLN6
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for CLN6 蛋白
ceroid-lipofuscinosis, neuronal 6 (Cln6) 蛋白CLN6, transmembrane ER protein (CLN6) 蛋白
CLN6, transmembrane ER protein S homeolog (cln6.S) 蛋白
ceroid-lipofuscinosis, neuronal 6, late infantile, variant (CLN6) 蛋白
CLN6, transmembrane ER protein (Cln6) 蛋白
CLN6, transmembrane ER protein a (cln6a) 蛋白
1810065L06Rik 蛋白
AW743417 蛋白
CLN4A 蛋白
cln6 蛋白
D9Bwg1455e 蛋白
HsT18960 蛋白
nclf 蛋白
zgc:103565 蛋白
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