USH1C antibody (AA 1-100)
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- Target See all USH1C Antibodies
- USH1C (Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C))
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Binding Specificity
- AA 1-100
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Reactivity
- Zebrafish (Danio rerio)
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This USH1C antibody is un-conjugated
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Application
- Western Blotting (WB)
- Sequence
- MERKVAREFR HKVELLIDNE AEKDYLYDVL RMYHQSMDLP VLVGDLKLVI NEPKRLPLFD AIRPLIPLKH QVQYDQLTPK RSRKLKEVRL DRTHPEGLGL
- Cross-Reactivity
- Human, Mouse, Rat
- Characteristics
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of zebrafish USH1C (NP_001035018.1).
- Isotype
- IgG
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anti-Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C) (AA 1-30), (N-Term) antibody
USH1C Reactivity: Human, Mouse WB Host: Rabbit Polyclonal RB41722 unconjugated
anti-Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C) (N-Term) antibodyVerified USH1C Reactivity: Human ELISA, WB, IHC Host: Goat Polyclonal unconjugated
anti-Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C) (AA 424-533) antibodyUSH1C Reactivity: Human ELISA, WB Host: Mouse Monoclonal 2B9 unconjugated
anti-Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C) (AA 424-533) antibodyUSH1C Reactivity: Human ELISA, WB, IP Host: Mouse Monoclonal 2B3 unconjugated
anti-Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C) (AA 1-533) antibodyUSH1C Reactivity: Human WB Host: Mouse Polyclonal unconjugated
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- Application Notes
- WB,1:200 - 1:2000
- Restrictions
- For Research Use only
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- 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.
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- Target
- USH1C (Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C))
- Alternative Name
- USH1C (USH1C Products)
- 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.,USH1C,AIE-75,DFNB18,DFNB18A,NY-CO-37,NY-CO-38,PDZ-45,PDZ-73,PDZ-73/NY-CO-38,PDZ73,PDZD7C,ush1cpst,harmonin,Cell Biology & Developmental Biology,Apoptosis,Neuroscience,USH1C
- Molecular Weight
- 45 kDa/58 kDa/60 kDa/62 kDa/101 kDa
- Gene ID
- 564412
- Pathways
- Sensory Perception of Sound
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