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CLN6
CLN6 transmembrane ER proteinFLJ20561, HsT18960, nclf
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]
Top validated antibodies |
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| Proteintech Group |  20315-1-AP |
1 references | Polyclonal |
WB
EL
ICC
IP
IHC
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| Invitrogen Antibodies | 20315-1-AP |
Polyclonal |
WB
ICC
IP
IHC
OA
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| LSBio | LS-C177359 |
Polyclonal |
WB
IHC
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| NovoPro Bioscience Inc. | 109397 |
Polyclonal |
WB
EL
ICC
IP
IHC
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| FineTest Biotech | FNab01768 |
Polyclonal |
WB
EL
ICC
IP
IHC
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