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Typical Testing Data/Standard Curve (for reference only) ()

Mouse Protein Wnt-10a ELISA Kit | Wnt10a elisa kit

Mouse Protein Wnt-10a ELISA Kit

Reactivity
Mouse
Synonyms
Protein Wnt-10a; Mouse Protein Wnt-10a ELISA Kit; Wnt10a; Wnt10a elisa kit
Ordering
For Research Use Only!
Reactivity
Mouse
Specificity
Recombinant and natural Mouse Protein Wnt-10a
Sequence Length
417
Samples
Serum, plasma, tissue homogenates, cell culture supernates or other biological fluids
Detection Range
0.156-10 ng/mL
Sensitivity
< 0.083 ng/mL
Intra-assay Precision
<=4.6%
Inter-assay Precision
<=6.4%
Preparation and Storage
For long term storage, please store the entire kit at -20 degree C.

Typical Testing Data/Standard Curve (for reference only)

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Typical Testing Data/Standard Curve (for reference only) ()
Related Product Information for Wnt10a elisa kit
Intended Uses: This immunoassay kit allows for the in vitro quantitative determination of target antigen concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

Principle of the Assay: The microtiter plate provided in this kit has been pre-coated with an antibody specific to target antigen. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for target antigen and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain target antigen, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of target antigen in the samples is then determined by comparing the O.D. of the samples to the standard curve.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
46,454 Da
NCBI Official Full Name
protein Wnt-10a
NCBI Official Synonym Full Names
wingless-type MMTV integration site family, member 10A
NCBI Official Symbol
Wnt10a
NCBI Protein Information
protein Wnt-10a
UniProt Protein Name
Protein Wnt-10a
Protein Family
UniProt Gene Name
Wnt10a
UniProt Entry Name
WN10A_MOUSE

Uniprot Description

WNT10A: Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule important in CNS development. Is likely to signal over only few cell diameters. Defects in WNT10A are a cause of ectodermal dysplasia anhidrotic (EDA); also known ectodermal dysplasia hypohidrotic autosomal recessive (HED). Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. EDA is characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands. Most patients carrying WNT10A mutations present with sweating anomalies. However, comparison with EDA cases harboring mutations in the ectodysplasin pathway identifies some phenotypic differences. Dermatological features (anomalies of hair and sweat glands) are less severe in patients carrying WNT10A mutations and facial dysmorphism can be absent. The dental phenotype consists in microdontia, whereas teeth agenesis is more frequent in patients carrying mutations in the ectodysplasin pathway. Defects in WNT10A are a cause of odonto-onycho-dermal dysplasia (OODD). OODD is a rare autosomal recessive ectodermal dysplasia in which the presenting phenotype is dry hair, severe hypodontia, smooth tongue with marked reduction of fungiform and filiform papillae, onychodysplasia, keratoderma and hyperhidrosis of palms and soles, and hyperkeratosis of the skin. Defects in WNT10A are a cause of Schopf-Schulz-Passarge syndrome (SSPS). SSPS is rare ectodermal dysplasia, characterized chiefly by cysts of the eyelid margins, palmoplantar keratoderma, hypodontia, hypotrichosis and nail dystrophy. Multiple eyelid apocrine hidrocystomas are the hallmark of this condition, although they usually appear in adulthood. The concomitant presence of eccrine syringofibroadenoma in most patients and of other adnexal skin tumors in some affected subjects indicates that Schopf-Schulz-Passarge syndrome is a genodermatosis with skin appendage neoplasms. Belongs to the Wnt family.

Protein type: Secreted; Secreted, signal peptide

Cellular Component: extracellular region; extracellular space; proteinaceous extracellular matrix

Molecular Function: frizzled binding; receptor binding

Biological Process: cell fate commitment; cell-cell signaling; epidermis morphogenesis; hair follicle development; hair follicle morphogenesis; multicellular organismal development; neural crest cell differentiation; neuron differentiation; odontogenesis; organ morphogenesis; regulation of odontogenesis of dentine-containing teeth; sebaceous gland development; signal transduction; skin development; tongue development; Wnt receptor signaling pathway

Research Articles on Wnt10a

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Product Notes

The Mouse Wnt10a wnt10a (Catalog #AAA2881760) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA2881760 ELISA Kit recognizes Mouse Wnt10a. It is sometimes possible for the material contained within the vial of "Protein Wnt-10a, 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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