Dfna5 deafness Antibody

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Immunohistochemistry: Dfna5 deafness Antibody [NB110-75027] - IHC on mouse brain using Rabbit antibody to mouse Dfna5 deafness-2 (non-syndromic hearing impairment protein 5 homolog): whole serum at 1 : 500 dilution, ...read more
Immunohistochemistry: Dfna5 deafness Antibody [NB110-75027] - IHC on mouse brain using Rabbit antibody to mouse Dfna5 deafness-2 (non-syndromic hearing impairment protein 5 homolog): whole serum at 1 : 500 dilution, ...read more

Product Details

Summary
Reactivity MuSpecies Glossary
Applications WB, IHC, IHC-Fr, IHC-P
Clonality
Polyclonal
Host
Rabbit
Conjugate
Unconjugated
Concentration
LYOPH

Order Details

Dfna5 deafness Antibody Summary

Immunogen
A synthetic peptide as a internal part of mouse Dfna5 deafness (non-syndromic hearing impairment protein 5 homolog) conjugated to immunogenic carrier protein was used as the immunogen.
Specificity
Dfna5 deafness.
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
DFNA5
Purity
Unpurified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Western Blot 1:300-1:3000
  • Immunohistochemistry 1:10-1:500
  • Immunohistochemistry-Frozen 1:10-1:500
  • Immunohistochemistry-Paraffin 1:10-1:500

Reactivity Notes

Mouse.

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
Whole antisera
Preservative
No Preservative
Concentration
LYOPH
Purity
Unpurified
Reconstitution Instructions
Reconstitute with 0.1 ml sterilized water to desired concentration.

Alternate Names for Dfna5 deafness Antibody

  • deafness, autosomal dominant 5
  • ICERE1
  • ICERE-1nonsyndromic hearing impairment protein
  • Inversely correlated with estrogen receptor expression 1
  • non-syndromic hearing impairment protein 5

Background

TISSUE SPECIFICITY: Expressed in cochlea. Low level of expression in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas, with highest expression in placenta.; DISEASE: Defects in DFNA5 are the cause of non-syndromic sensorineural deafness autosomal dominant type 5 (Dfna5). Dfna5 deafness is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.

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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Video Protocols

WB Video Protocol

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Secondary Antibodies

 

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Bioinformatics

Gene Symbol DFNA5
Entrez
Uniprot