CLN5 rabbit pAb
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CLN5 rabbit pAb
Background :
Ceroid-lipofuscinosis, neuronal 5 (CLN5) Homo sapiens 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]Description :
Ceroid-lipofuscinosis, neuronal 5 (CLN5) Homo sapiens 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],Product Name Alternative :
CLN5; Ceroid-lipofuscinosis neuronal protein 5; Protein CLN5UniProt :
O75503Swiss Prot :
O75503Reactivity :
Human; Mouse; RatImmunogen :
The antiserum was produced against synthesized peptide derived from human CLN5. AA range:171-220Target :
CLN5Clonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.Buffer :
-20°C/1 yearMolecular Weight :
48kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
48kDFragment :
IgGSubcellular Location :
[Ceroid-lipofuscinosis neuronal protein 5, secreted form]: Lysosome .; [Ceroid-lipofuscinosis neuronal protein 5]: Membrane ; Single-pass type II membrane protein . An amphipathic anchor region facilitates its association with the membrane. .Other Product Names :
CLN5; Ceroid-lipofuscinosis neuronal protein 5; Protein CLN5Gene ID (Human) :
1203

