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USH1G antibody (Internal Region)

This anti-USH1G antibody is a Rabbit Polyclonal antibody detecting USH1G in ELISA, WB, ICC and IF. Suitable for Human and Mouse.
Catalog No. ABIN4889610

Quick Overview for USH1G antibody (Internal Region) (ABIN4889610)

Target

See all USH1G Antibodies
USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Reactivity

Human, Mouse

Host

  • 7
Rabbit

Clonality

  • 7
Polyclonal

Conjugate

  • 3
  • 2
  • 1
  • 1
This USH1G antibody is un-conjugated

Application

ELISA, Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • Binding Specificity

    Internal Region

    Specificity

    Reacts with human and mouse USH1G

    Purification

    Purified (protein A)

    Immunogen

    Synthetic peptide of derived from internal part of human USH1G.
  • Application Notes

    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
  • 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
  • Target

    USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

    Alternative Name

    USH1G

    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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