USH1G antibody (Internal Region)
USH1G
Reactivity: Human, Mouse
ELISA, WB, ICC, IF
Host: Rabbit
Polyclonal
unconjugated
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- Target See all USH1G Antibodies
- USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
- Binding Specificity
- Internal Region
- Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This USH1G antibody is un-conjugated
- Application
- ELISA, Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
- Specificity
- Reacts with human and mouse USH1G
- Purification
- Purified (protein A)
- Immunogen
- Synthetic peptide of derived from internal part of human USH1G.
- Top Product
- Discover our top product USH1G Primary Antibody
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- Application Notes
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Working dilution: Optimal dilutions should be determined by the end user.
The following are guidelines only:
- WB : 1/500 to 1/2000 - ICC, IF: 1/200 to 1/1000 - Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Must be reconstituted in distilled water.
- Concentration
- 1 mg/mL
- Buffer
- Tris 0,1M, glycine 0,1M
- Storage
- 4 °C/-20 °C
- Storage Comment
- Short term storage at+4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.
- Expiry Date
- 6 months
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- Target
- USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
- Alternative Name
- USH1G (USH1G Products)
- Synonyms
- ANKS4A antibody, SANS antibody, Sans antibody, js antibody, USH1 protein network component sans antibody, USH1G antibody, Ush1g antibody
- Background
- Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.
- Gene ID
- 124590
- UniProt
- Q495M9
- Pathways
- Sensory Perception of Sound
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