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DFNA5 antibody
DFNA5
Reactivity: Human, Rat, Mouse
WB, ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-DFNA5 Antibody
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Target
See all DFNA5 Antibodies
DFNA5
(Deafness, Autosomal Dominant 5 (DFNA5))
Reactivity
All reactivities for DFNA5 antibodies
Human, Rat, Mouse
Host
All hosts for DFNA5 antibodies
Rabbit
Clonality
All clonalities for DFNA5 antibodies
Polyclonal
Conjugate
All conjugates for DFNA5 antibodies
This DFNA5 antibody is un-conjugated
Application
All applications for DFNA5 antibodies
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
Purification
Immunogen affinity purified
Purity
≥95 % as determined by SDS-PAGE
Immunogen
deafness, autosomal dominant 5
Isotype
IgG
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Discover our top product DFNA5 Primary Antibody
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Application Details
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Application Notes
WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
-20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Expiry Date
12 months
Target Details for DFNA5
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Target
DFNA5
(Deafness, Autosomal Dominant 5 (DFNA5))
Alternative Name
DFNA5 (DFNA5 Products )
Synonyms
Dfna5h antibody, fk59f08 antibody, zgc:91916 antibody, wu:fc41e05 antibody, wu:fk59f08 antibody, MGC83660 antibody, ICERE-1 antibody, 2310037D07Rik antibody, 4932441K13Rik antibody, EG14210 antibody, Fin15 antibody, gasdermin E antibody, gasdermin Eb antibody, DFNA5, deafness associated tumor suppressor antibody, gasdermin E L homeolog antibody, Gsdme antibody, gsdmeb antibody, DFNA5 antibody, gsdme.L antibody, GSDME antibody
Background
Synonyms:deafness, autosomal dominant 5, DFNA5, ICERE 1, ICERE1 Background:Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.
Molecular Weight
Refer to figures
Gene ID
1687
UniProt
O60443
Pathways
Sensory Perception of Sound
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