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DFNB31 antibody (Middle Region)
This anti-DFNB31 antibody is a Rabbit Polyclonal antibody detecting DFNB31 in WB, IHC (p) and EIA. Suitable for Human.
Quick Overview for DFNB31 antibody (Middle Region) (ABIN955575)
Target
See all DFNB31 Antibodies
DFNB31
(Deafness, Autosomal Recessive 31 (DFNB31))
Reactivity
All reactivities for DFNB31 antibodies
Human
Host
All hosts for DFNB31 antibodies
Rabbit
Clonality
All clonalities for DFNB31 antibodies
Polyclonal
Conjugate
All conjugates for DFNB31 antibodies
This DFNB31 antibody is un-conjugated
Application
All applications for DFNB31 antibodies
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
Product Details anti-DFNB31 Antibody
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Binding Specificity
All epitopes for DFNB31 antibodies
AA 385-413, Middle Region
Specificity
This antibody recognizes Human Whirlin (Center).
Purification
Affinity Chromatography on Protein A
Immunogen
KLH conjugated synthetic peptide between 385-413 amino acids from the Central region of Human Whirlin. Genename: WHRN
Isotype
Ig Fraction
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS, 0.09 % Sodium Azide
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Target Details for DFNB31
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Target
DFNB31
(Deafness, Autosomal Recessive 31 (DFNB31))
Alternative Name
Whirlin
Background
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.Synonyms: Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN
Molecular Weight
96586 Da
Gene ID
25861
NCBI Accession
NP_001077354
Pathways
Sensory Perception of Sound
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