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Human Dyslexia-associated protein KIAA0319 ELISA Kit | KIAA0319 elisa kit

Human Dyslexia-associated protein KIAA0319 (KIAA0319) ELISA Kit

Gene Names
KIAA0319; AAVR; DYX2; NMIG; DYLX2
Reactivity
Human
Synonyms
Dyslexia-associated protein KIAA0319; Human Dyslexia-associated protein KIAA0319 (KIAA0319) ELISA Kit; DLX2; DYLX2; DYX2; MGC176717; dyslexia susceptibility 2; KIAA0319 elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Specificity
This assay has high sensitivity and excellent specificity for detection of Human KIAA0319. No significant cross-reactivity or interference between Human KIAA0319 and analogues was observed.
Sequence Length
970
Samples
Serum, Plasma, Other biological fluids
Assay Type
Sandwich
Sample Volume
1-200 uL
Precision
Intra-assay Precision (Precision within an assay)
Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.
Inter-assay Precision (Precision between assays)
Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.
CV (%) = SD/meanX100
Intra-Assay: CV
Inter-Assay: CV
Detection Wavelength
450 nm
Preparation and Storage
Store at 2-8 degree C.
Related Product Information for KIAA0319 elisa kit
Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate KIAA0319 in samples. An antibody specific for KIAA0319 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyKIAA0319 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for KIAA0319 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of KIAA0319 bound in the initial step. The color development is stopped and the intensity of the color is measured.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
110,370 Da
NCBI Official Full Name
dyslexia-associated protein KIAA0319 isoform b
NCBI Official Synonym Full Names
KIAA0319
NCBI Official Symbol
KIAA0319
NCBI Official Synonym Symbols
AAVR; DYX2; NMIG; DYLX2
NCBI Protein Information
dyslexia-associated protein KIAA0319
UniProt Protein Name
Dyslexia-associated protein KIAA0319
UniProt Gene Name
KIAA0319

NCBI Description

This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in this gene are associated with dyslexia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]

Uniprot Description

KIAA0319: Involved in neuronal migration during development of the cerebral neocortex. May function in a cell autonomous and a non- cell autonomous manner and play a role in appropriate adhesion between migrating neurons and radial glial fibers. May also regulate growth and differentiation of dendrites. Defects in KIAA0319 may be a cause of susceptibility to dyslexia type 2 (DYX2); also known as specific reading disability type 2. Dyslexia is a relatively common, complex cognitive disorder that affects 5% to 10% of school-aged children. The disorder is characterized by an impairment of reading performance despite adequate motivational, educational and intellectual opportunities and in the absence of sensory or neurological disability. A lower expression is associated with the risk haplotype. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral

Chromosomal Location of Human Ortholog: 6p22.3

Cellular Component: clathrin-coated vesicle membrane; early endosome; early endosome membrane; integral component of membrane; plasma membrane

Molecular Function: protein binding

Biological Process: neuron migration

Disease: Dyslexia, Susceptibility To, 2

Research Articles on KIAA0319

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Product Notes

The Human KIAA0319 kiaa0319 (Catalog #AAA285964) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA285964 ELISA Kit recognizes Human KIAA0319. It is sometimes possible for the material contained within the vial of "Dyslexia-associated protein KIAA0319, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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