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Myosin VIIa Antibody (31A12)

Novus Biologicals, part of Bio-Techne | Catalog # NBP3-26121

Recombinant monoclonal antibody expressed in HEK293F cells
Novus Biologicals, part of Bio-Techne
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NBP3-26121-100ul
NBP3-26121-50ul

Key Product Details

Species Reactivity

Human

Applications

ELISA, Flow Cytometry

Label

Unconjugated

Antibody Source

Recombinant Monoclonal Rabbit IgG Clone # 31A12

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Product Specifications

Immunogen

A synthesized peptide derived from Human Myosin VIIa [UniProt Q13402]

Clonality

Monoclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for Myosin VIIa Antibody (31A12)

Myosin VIIa Antibody (31A12)

Flow Cytometry: Myosin VIIa Antibody (31A12) [NBP3-26121] -

Flow Cytometry: Myosin VIIa Antibody (31A12) [NBP3-26121] - Overlay Peak curve showing HepG2 cells stained with Myosin VIIa Antibody (31A12) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.

Applications for Myosin VIIa Antibody (31A12)

Application
Recommended Usage

Flow Cytometry

1:50-1:200

Formulation, Preparation, and Storage

Purification

Affinity purified

Formulation

PBS, pH 7.4, 150mM NaCl and 50% glycerol

Preservative

0.02% Sodium Azide

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at -20 to -70C. Avoid freeze-thaw cycles.

Background: Myosin VIIa

Myosin VIIa is a member of the myosin superfamily of actin-based motor proteins. Defects in the myosin VIIa gene are responsible for hearing impairment in shaker-1 (sh1) mice and causes Usher syndrome IB in humans. Usher syndrome associates congenital deafness, vestibular dysfunction, and retinitis pigmentosa and is the most common form of combined deafness and blindness. Structural features of myosin VIIa protein include an ATP binding N-terminal motor domain, a central region which possess five light-chain binding (IQ) motifs, and a C-terminal domain with three myosin tail homology (MyTH4) and talin-like homology regions.

Alternate Names

deafness, autosomal dominant 11, deafness, autosomal recessive 2, DFNA11, DFNB2, myosin VIIA, myosin-VIIa, MYOVIIA, MYU7A, USH1Bsevere))

Gene Symbol

MYO7A

Additional Myosin VIIa Products

Product Documents for Myosin VIIa Antibody (31A12)

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for Myosin VIIa Antibody (31A12)

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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