USH1C antibody (AA 1-100)

Catalog No. ABIN1683223

Product Details anti-USH1C Antibody

Target: USH1C (Usher Syndrome 1C (Autosomal Recessive, Severe) (USH1C))

Binding Specificity: AA 1-100

Reactivity: Zebrafish (Danio rerio)

Host: Rabbit

Clonality: Polyclonal

Conjugate: This USH1C antibody is un-conjugated

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

Application Details

Application Notes: WB,1:200 - 1:2000

Restrictions: For Research Use only

Handling

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

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.,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