Product Name
Battenin (CLN3), ELISA Kit
Full Product Name
Rabbit Battenin (CLN3) ELISA Kit
Product Gene Name
CLN3 elisa kit
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
Species Reactivity
Rabbit
Samples
Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate
Preparation and Storage
Store all reagents at 2-8 degree C.
Sample Preparation
We suggest pre-experimenting with neat (undiluted) samples, 1:2 or 1:4 dilutions. Please avoid diluting your samples more than 1:10 as it would exceed the dilution limit set for this kit. If the expected concentration of the target is beyond the detection range of the kit, please contact our technical support team
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of CLN3 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for CLN3 purchase
MBS7223527 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Battenin (CLN3) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing CLN3. The ELISA analytical biochemical technique of the MBS7223527 kit is based on CLN3 antibody-CLN3 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect CLN3 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, CLN3. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
Product Categories/Family for CLN3 elisa kit
Neurobiology
NCBI/Uniprot data below describe general gene information for CLN3. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001035897.1
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NCBI GenBank Nucleotide #
NM_001042432.1
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UniProt Secondary Accession #
O00668; O95089; Q549S9; Q9UP09; Q9UP11; Q9UP12; Q9UP13; Q9UP14; B2R7J1[Other Products]
UniProt Related Accession #
Q13286[Other Products]
Molecular Weight
37,969 Da
NCBI Official Full Name
battenin isoform a
NCBI Official Synonym Full Names
ceroid-lipofuscinosis, neuronal 3
NCBI Official Symbol
CLN3??[Similar Products]
NCBI Official Synonym Symbols
BTS; JNCL
??[Similar Products]
NCBI Protein Information
battenin; batten disease protein
UniProt Protein Name
Battenin
UniProt Synonym Protein Names
Batten disease protein; Protein CLN3
UniProt Gene Name
CLN3??[Similar Products]
UniProt Synonym Gene Names
BTS??[Similar Products]
UniProt Entry Name
CLN3_HUMAN
NCBI Summary for CLN3
This gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]
UniProt Comments for CLN3
CLN3: Involved in microtubule-dependent, anterograde transport of late endosomes and lysosomes. Defects in CLN3 are the cause of neuronal ceroid lipofuscinosis type 3 (CLN3); also known as Batten disease. A form of neuronal ceroid lipofuscinosis. Neuronal ceroid lipofuscinoses are progressive neurodegenerative, lysosomal storage diseases characterized by intracellular accumulation of autofluorescent liposomal material, and clinically by seizures, dementia, visual loss, and/or cerebral atrophy. The hallmark of CLN3 is the ultrastructural pattern of lipopigment with a fingerprint profile, which can have 3 different appearances: pure within a lysosomal residual body; in conjunction with curvilinear or rectilinear profiles; and as a small component within large membrane-bound lysosomal vacuoles. The combination of fingerprint profiles within lysosomal vacuoles is a regular feature of blood lymphocytes from patients with CLN3. Belongs to the battenin family. 5 isoforms of the human protein are produced by alternative splicing.
Protein type: Apoptosis; Autophagy; Chaperone; Membrane protein, multi-pass; Membrane protein, integral; Vesicle; Mitochondrial
Chromosomal Location of Human Ortholog: 16p12.1
Cellular Component: Golgi apparatus; neuron projection; Golgi stack; mitochondrion; endoplasmic reticulum; lysosome; lysosomal membrane; early endosome; integral to membrane; autophagic vacuole; caveola; trans-Golgi network; lipid raft; Golgi membrane; synaptic vesicle; late endosome; cytoplasm; plasma membrane; integral to endoplasmic reticulum membrane; nucleus
Molecular Function: protein binding; unfolded protein binding
Biological Process: sphingomyelin metabolic process; autophagic vacuole fusion; macroautophagy; glucosylceramide metabolic process; negative regulation of macroautophagy; amyloid precursor protein catabolic process; neurotransmitter metabolic process; vesicle transport along microtubule; protein catabolic process; negative regulation of neuron apoptosis; neuromuscular process controlling balance; associative learning; amino acid metabolic process; negative regulation of proteolysis; receptor-mediated endocytosis; regulation of action potential; cytosolic calcium ion homeostasis; vacuolar transport; arginine transport; globoside metabolic process; galactosylceramide metabolic process; ionotropic glutamate receptor signaling pathway; lysosome organization and biogenesis; negative regulation of catalytic activity; lysosomal lumen acidification; protein processing; ceramide metabolic process; negative regulation of apoptosis
Disease: Ceroid Lipofuscinosis, Neuronal, 3
Research Articles on CLN3
1. Genetic testing for CLN3 should be considered in autophagic vacuolar myopathy (AVM), with autophagic vacuoles and sarcolemmal features.
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