Myosin VIIa Antibody

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Product Details

Summary
Product Discontinued
View other related Myosin VIIa Primary Antibodies

Order Details


    • Catalog Number
      NBP1-84266
    • Availability
      Product Discontinued

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Myosin VIIa Antibody Summary

Immunogen
This antibody was developed against Recombinant Protein corresponding to amino acids: WAVLTVQAYARGMIARRLHQRLRAEYLWRLEAEKMRLAEEEKLRKEMSAKKAKEEAERKHQERLAQLAREDAERELKEKEAARRKKELLEQMERARHEPVNHSDMVDKMFGFLGTSGGLPGQEGQAPSGFE
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
MYO7A
Purity
Immunogen affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunocytochemistry/ Immunofluorescence 1 - 4 ug/ml
  • Immunohistochemistry 1:200 - 1:500
  • Immunohistochemistry-Paraffin 1:200 - 1:500
Application Notes
ICC/IF reported in scientific literature (PMID: 25760435). For IHC-Paraffin, HIER pH 6 retrieval is recommended. ICC/IF Fixation Permeabilization: Use PFA/Triton X-100.
Publications
Read Publications using
NBP1-84266 in the following applications:

Reactivity Notes

Mouse reactivity reported in scientific literature (PMID: 28241887). Guinea Pig reactivity reported in the literature (PMID: 29945803)

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.2) and 40% Glycerol
Preservative
0.02% Sodium Azide
Purity
Immunogen affinity purified

Alternate Names for Myosin VIIa Antibody

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

Background

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.

Limitations

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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Publications for Myosin VIIa Antibody (NBP1-84266)(6)

We have publications tested in 3 confirmed species: Human, Mouse, Guinea Pig.

We have publications tested in 2 applications: ICC/IF, IF/IHC.


Filter By Application
ICC/IF
(2)
IF/IHC
(4)
All Applications
Filter By Species
Human
(3)
Mouse
(2)
Guinea Pig
(1)
All Species

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Product General Protocols

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Video Protocols

ICC/IF Video Protocol

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol MYO7A