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].

Recommended next Filters:

More filter options

您想试用我们的人工智能搜索吗？

显示筛选器

5 results

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

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)

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

3 images

产品编号 ABIN7546597

获取报价

详细

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

CLN6 宿主: 人宿主: 小麦胚 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

产品编号 ABIN1349721

获取报价

详细

CLN6 Protein (GST tag,His tag)

CLN6 宿主: 人宿主: 大肠杆菌（E. Coli） Recombinant ELISA, WB, SDS

产品编号 ABIN7576223

获取报价

详细

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

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

产品编号 ABIN3107550

获取报价

详细