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Typical Testing Data/Standard Curve (for reference only) (Fig.1. Human Myosin-VIIa (MYO7A) Standard Curve.)

Human Myosin-VIIa (MYO7A) ELISA Kit | MYO7A elisa kit

Human Myosin-VIIa (MYO7A) ELISA Kit

Gene Names
MYO7A; DFNB2; MYU7A; NSRD2; USH1B; DFNA11; MYOVIIA
Reactivity
Human
Synonyms
Myosin-VIIa (MYO7A); Human Myosin-VIIa (MYO7A) ELISA Kit; MYO7A; DFNA11; DFNB2; MYOVIIA; MYU7A; NSRD2; USH1B; deafness; autosomal dominant 11; autosomal recessive 2; myosin VIIA (Usher syndrome 1B (autosomal recessive; severe)); MYO7A elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Specificity
Human Myosin-VIIa (MYO7A) ELISA Kit has high sensitivity and excellent specificity for detection of Human MYO7A. No significant cross-reactivity or interference between Human MYO7A and analogues was observed.
Sequence Length
2215
Assay Type
Sandwich
Preparation and Storage
Store at 2-8 degree C.

Typical Testing Data/Standard Curve (for reference only)

(Fig.1. Human Myosin-VIIa (MYO7A) Standard Curve.)

Typical Testing Data/Standard Curve (for reference only) (Fig.1. Human Myosin-VIIa (MYO7A) Standard Curve.)
Related Product Information for MYO7A elisa kit
Principle of the Assay: Human Myosin-VIIa (MYO7A) ELISA Kit employs a two-site sandwich ELISA to quantitate MYO7A in samples. An antibody specific for Human MYO7A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any MYO7A present is bound by the immobilized antibody. After removing any unbound substances, HRP-Conjugated MYO7A detection antibody is added to the wells. Following a wash to remove any unbound HRP reagent, a Chromogen solution is added to the wells and color develops in proportion to the amount of MYO7A 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
UniProt Accession #
NCBI Official Full Name
Unconventional myosin-VIIa
NCBI Official Synonym Full Names
myosin VIIA
NCBI Official Symbol
MYO7A
NCBI Official Synonym Symbols
DFNB2; MYU7A; NSRD2; USH1B; DFNA11; MYOVIIA
NCBI Protein Information
unconventional myosin-VIIa
UniProt Protein Name
Unconventional myosin-VIIa
Protein Family
UniProt Gene Name
MYO7A
UniProt Synonym Gene Names
USH1B
UniProt Entry Name
MYO7A_HUMAN

NCBI Description

This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]

Uniprot Description

MYO7A: an actin-based motor molecule with ATPase activity and a calcium sensitive calmodulin binding subunit. May play a role in trafficking of ribbon- synaptic vesicle complexes and renewal of outer photoreceptor disks. Involved in hair-cell vesicle trafficking of aminoglycosides, which are known to induce ototoxicity. Seven alternatively spliced isoforms have been described.

Protein type: Motor; Motility/polarity/chemotaxis

Chromosomal Location of Human Ortholog: 11q13.5

Cellular Component: stereocilium; photoreceptor inner segment; photoreceptor outer segment; lysosomal membrane; cytoplasm; apical plasma membrane; melanosome; synapse; cell cortex; cytosol; photoreceptor connecting cilium

Molecular Function: actin filament binding; microfilament motor activity; calmodulin binding; protein domain specific binding; protein binding; protein homodimerization activity; spectrin binding; ADP binding; actin-dependent ATPase activity; ATP binding

Biological Process: phagolysosome formation; intracellular protein transport; eye photoreceptor cell development; sensory perception of sound; pigment granule transport; visual perception; actin filament-based movement; lysosome organization and biogenesis; metabolic process; sensory perception of light stimulus; auditory receptor cell stereocilium organization and biogenesis; equilibrioception; post-embryonic organ morphogenesis

Disease: Deafness, Autosomal Dominant 11; Deafness, Autosomal Recessive 2; Usher Syndrome, Type I

Research Articles on MYO7A

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Product Notes

The Human MYO7A myo7a (Catalog #AAA9715077) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9715077 ELISA Kit recognizes Human MYO7A. It is sometimes possible for the material contained within the vial of "Myosin-VIIa (MYO7A), 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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