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USH1C antibody
USH1C
Reactivity: Human, Mouse, Rat
IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-USH1C Antibody
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Target
See all USH1C Antibodies
USH1C
(Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C))
Reactivity
All reactivities for USH1C antibodies
Human, Mouse, Rat
Host
All hosts for USH1C antibodies
Rabbit
Clonality
All clonalities for USH1C antibodies
Polyclonal
Conjugate
All conjugates for USH1C antibodies
This USH1C antibody is un-conjugated
Application
All applications for USH1C antibodies
Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of zebrafish USH1C (NP_001035018.1).
Isotype
IgG
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Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 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
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for USH1C
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Target
USH1C
(Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C))
Alternative Name
USH1C (USH1C Products )
Synonyms
AIE-75 antibody, DFNB18 antibody, DFNB18A antibody, NY-CO-37 antibody, NY-CO-38 antibody, PDZ-45 antibody, PDZ-73 antibody, PDZ-73/NY-CO-38 antibody, PDZ73 antibody, PDZD7C antibody, ush1cpst antibody, 2010016F01Rik antibody, harmonin antibody, zgc:136806 antibody, ush1c antibody, USH1 protein network component harmonin antibody, harmonin antibody, Usher syndrome 1C antibody, USH1 protein network component harmonin L homeolog antibody, USH1C antibody, CpipJ_CPIJ012732 antibody, Ush1c antibody, ush1c antibody, ush1c.L antibody
Background
This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene.
Gene ID
564412
UniProt
Q9ES64
Pathways
Sensory Perception of Sound
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