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CLN5


Official Full Name
CLN5 intracellular trafficking protein
Organism
Homo sapiens
Gene ID
1203
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]
Synonyms
Defb3; BD-3

Cat.No. Product Name Price
SHH265497 shRNA set against Mouse CLN5 (NM_001033242.1) Inquiry
SHG183511 shRNA set against Mouse Cln5(NM_001033242.1) Inquiry
SHH265493 shRNA set against Human CLN5 (NM_006493.2) Inquiry
SHW004381 shRNA set against Chicken CLN5 (NM_001282194) Inquiry
Cat.No. Product Name Price
CDCH383451 Human CLN5 ORF clone(NM_006493.2) Inquiry
MiUTR1M-03104 CLN5 miRNA 3'UTR clone Inquiry
MiUTR3H-09736 CLN5 miRNA 3'UTR clone Inquiry
CDCB165856 Chicken CLN5 ORF Clone (NM_001282194) Inquiry
CDCB191289 Rabbit CLN5 ORF clone (XM_002712933.2) Inquiry
CDCH383453 Rat CLN5 ORF clone(NM_001191689.1) Inquiry
CDCR048232 Mouse Cln5 ORF clone (NM_001033242.1) Inquiry
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