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CLN5 Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501981607
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100 μL
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50-198-1607 100 μL
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Catalog No. 50-198-1607 Supplier Bioss Supplier No. BS11714R
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Rabbit Polyclonal Antibody

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].

Specifications

Antigen CLN5
Applications Western Blot
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene CLN5
Gene Accession No. O75503
Gene Alias A730075N08Rik; Ceroid-lipofuscinosis neuronal protein 5; Ceroid-lipofuscinosis neuronal protein 5 homolog; Ceroid-lipofuscinosis neuronal protein 5 homolog, secreted form; Ceroid-lipofuscinosis neuronal protein 5, secreted form; ceroid-lipofuscinosis, neuronal 5; CLN5; NCL; Protein CLN5
Gene Symbols CLN5
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human CLN5.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 1203
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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