USH1G antibody
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- Target See all USH1G Antibodies
- USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This USH1G antibody is un-conjugated
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Human
- Purification
- Purified by antigen-affinity chromatography.
- Immunogen
- Recombinant protein encompassing a sequence within the center region of human USH1G. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product USH1G Primary Antibody
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- Application Notes
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Comment
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Positive Control: A431
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal
- Preservative
- Thimerosal (Merthiolate)
- Precaution of Use
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C,-20 °C
- Storage Comment
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Target
- USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
- Alternative Name
- USH1 protein network component sans (USH1G Products)
- Synonyms
- ANKS4A antibody, SANS antibody, Sans antibody, js antibody, USH1 protein network component sans antibody, USH1G antibody, Ush1g antibody
- Background
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Synonyms: USH1 protein network component sans , ANKS4A , SANS
Background: This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G). [provided by RefSeq]
- Molecular Weight
- 51 kDa
- Gene ID
- 124590
- UniProt
- Q495M9
- Pathways
- Sensory Perception of Sound
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