Myosin VIIa Antibody - BSA Free

Novus Biologicals, part of Bio-Techne | Catalog # NBP3-46966

Novus Biologicals, part of Bio-Techne
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NBP3-46966
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Key Product Details

Species Reactivity

Human, Mouse, Rat

Applications

ELISA, Immunocytochemistry/ Immunofluorescence, Western Blot

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free

Concentration

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

View all Myosin VIIa Antibodies »

Product Specifications

Immunogen

myosin VIIA. (Uniprot# Q13402)

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Description

Novus Biologicals Rabbit Myosin VIIa Antibody - BSA Free (NBP3-46966) is a polyclonal antibody validated for use in WB, ELISA and ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee.

Scientific Data Images for Myosin VIIa Antibody - BSA Free

Myosin VIIa Antibody - BSA Free

Western Blot: Myosin VIIa Antibody - BSA Free [NBP3-46966] -

Western Blot: Myosin VIIa Antibody - BSA Free [NBP3-46966] - L02 cells were subjected to SDS PAGE followed by western blot with (Myosin VIIa antibody) at dilution of 1:500

Applications for Myosin VIIa Antibody - BSA Free

Application
Recommended Usage

Immunocytochemistry/ Immunofluorescence

1:20-1:200

Western Blot

1:500-1:2000
Application Notes
Theoretical Molecular Weight is 160-255 kDa

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

PBS, 50% Glycerol, pH (7.3)

Format

BSA Free

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 -20C. 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 - BSA Free

Product Datasheets

Certificate of Analysis

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Product Specific Notices for Myosin VIIa Antibody - BSA Free

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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