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Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) ELISA Kits

CLN5 is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Additionally we are shipping CLN5 Antibodies (44) and CLN5 Proteins (6) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human CLN5 CLN5 1203 O75503
Anti-Mouse CLN5 CLN5 211286 Q3UMW8
Anti-Rat CLN5 CLN5 306128  
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More ELISA Kits for CLN5 Interaction Partners

Human Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) interaction partners

  1. findings support CLN5 hypomorphic mutations cause autosomal recessive cerebellar ataxia (show USP14 ELISA Kits), confirming other reports showing CLN (show CLGN ELISA Kits) mutations are associated with adult-onset neurodegenerative disorders

  2. Two forms of CLN5, derived from the C-terminal proteolytic processing, are present in most cells and tissues.

  3. There are functional differences in various N-glycosylation sites of CLN5 which affect folding, trafficking, and lysosomal function of CLN5.

  4. a role for CLN5 in controlling the itinerary of the lysosomal sorting receptors by regulating retromer recruitment at the endosome

  5. This study highlights a close interaction between CLN5/CLN8 (show CLN8 ELISA Kits) proteins, and their role in sphingolipid metabolism. Our findings suggest that CLN5p/CLN8p most likely are positive modulators of CerS1 (show CERS1 ELISA Kits) and/or CerS2 (show CERS2 ELISA Kits).

  6. analysis of mutations in neuronal ceroid lipofuscinosis (show CLN6 ELISA Kits) protein CLN5

  7. CLN5 mutations are 1 (show VPS52 ELISA Kits)) more common in patients with neuronal ceroid lipofuscinosis (show CLN6 ELISA Kits) (NCL) than previously reported, 2) found in patients of broad ethnic diversity, and 3) can be identified in patients with disease onset in adult and juvenile epochs

  8. Study found that CLN5 interacts with several other NCL proteins namely, CLN1/PPT1 (show PPT1 ELISA Kits), CLN2/TPP1 (show TPP1 ELISA Kits), CLN3 (show CLN3 ELISA Kits), CLN6 (show CLN6 ELISA Kits) and CLN8 (show CLN8 ELISA Kits).

  9. juvenile and variant late infantile neuronal ceroid lipofuscinoses have mutated CLN (show CLGN ELISA Kits) genes encoding lysosomal proteins (review)

  10. Data show that three neuronal ceroid lipofuscinoses disease forms with similar tissue pathology are connected at the molecular level: CLN5 polypeptides directly interact with the CLN2 (show TPP1 ELISA Kits) and CLN3 (show CLN3 ELISA Kits) proteins

Mouse (Murine) Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) interaction partners

  1. Rssults suggested that CLN2 (show TPP1 ELISA Kits), CLN3 (show CLN3 ELISA Kits) and CLN5 genes may play an important role in early embryonal neurogenesis.

  2. The simultaneous loss of both Cln1 (show PPT1 ELISA Kits) and Cln5 genes might enhance the typical pathological phenotypes of these mice by disrupting or downregulating shared or convergent pathogenic pathways.

  3. In Cln5-deficient mice, early and significant microglial activation is documented that is already evident at 3 months of age; it increases gradually with age and differs between neurons and glia, with the highest expression in microglia.

  4. Study found that CLN5 interacts with several other NCL (show NCL ELISA Kits) proteins namely, CLN1/PPT1 (show PPT1 ELISA Kits), CLN2/TPP1 (show TPP1 ELISA Kits), CLN3 (show CLN3 ELISA Kits), CLN6 (show CLN6 ELISA Kits) and CLN8 (show CLN8 ELISA Kits).

  5. Mouse Cln5 is a soluble lysosomal glycoprotein expressed throughout embryonic brain, increasing during development; prominent expression is observed in cerebellar Purkinje cells, cerebral neurons, hippocampal pyramidal cells, and hippocampal interneurons.

  6. because the role of the functionally uncharacterized Cln5 protein remains unclear these studies may offer clues to the unraveling of its possible function(s)

  7. In mouse cerebral cortex, microinjection of VEGF-A (show VEGFA ELISA Kits) disrupted CLN-5 and OCLN (show OCLN ELISA Kits) and induced loss of barrier function

  8. These data provide unexpected evidence for a distinctive sequence of neuron loss in the thalamocortical system of Cln5-/- mice, diametrically opposed to that seen in other forms of NCL (show NCL ELISA Kits).

Cow (Bovine) Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) interaction partners

  1. The candidate genes for bovine Neuronal Ceroid Lipofuscinosis (show CLN6 ELISA Kits),CLN3 (show CLN3 ELISA Kits) , CLN5 and CLN6 (show CLN6 ELISA Kits), have been mapped to facilitate linkage analysis in cattle and sheep.

CLN5 Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with CLN5

  • ceroid-lipofuscinosis, neuronal 5 (CLN5) antibody
  • ceroid-lipofuscinosis, neuronal 5 (Cln5) antibody
  • CLN5 (LOC100152208) antibody
  • A730075N08Rik antibody
  • NCL antibody

Protein level used designations for CLN5

ceroid-lipofuscinosis neuronal protein 5 , ceroid-lipofuscinosis neuronal protein 5 homolog , ceroid-lipofuscinosis neuronal 5

GENE ID SPECIES
1203 Homo sapiens
211286 Mus musculus
529186 Bos taurus
485498 Canis lupus familiaris
100034668 Ovis aries
306128 Rattus norvegicus
100152208 Sus scrofa
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