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CLN6 Protéines

(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 Protein (AA 1-311) (His tag)

custom-made CLN6 Origine: Humain Hôte: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)

AlphaFold protein structure predicition of Human Recombinant CLN6 Protein, UniprotID Q9NWW5

3 images

N° du produit ABIN7546597

Détails

CLN6 Protein (AA 1-311) (GST tag)

CLN6 Origine: Humain Hôte: Wheat germ Recombinant ELISA, WB, AA, AP

Image no. 1 for Ceroid-Lipofuscinosis, Neuronal 6, Late Infantile, Variant (CLN6) (AA 1-311) protein (GST tag) (ABIN1349721)

1 image

N° du produit ABIN1349721

Détails

CLN6 Protein (GST tag,His tag)

CLN6 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant ELISA, WB, SDS

N° du produit ABIN7576223

Détails

CLN6 Protein (AA 1-311) (Strep Tag)

custom-made CLN6 Origine: Humain Hôte: Cell-free protein synthesis (CFPS) Recombinant approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC). ELISA, WB, SDS

N° du produit ABIN3107550