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Rhodopsin antibody (AA 310-339)

This Rabbit Polyclonal antibody specifically detects Rhodopsin in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN3032473

Quick Overview for Rhodopsin antibody (AA 310-339) (ABIN3032473)

Target

See all Rhodopsin (RHO) Antibodies
Rhodopsin (RHO)

Reactivity

  • 41
  • 20
  • 17
  • 13
  • 10
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 42
  • 25
  • 2
  • 1
  • 1
Rabbit

Clonality

  • 38
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Polyclonal

Conjugate

  • 31
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  • 3
  • 3
  • 2
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  • 2
  • 2
  • 2
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  • 2
This Rhodopsin antibody is un-conjugated

Application

  • 52
  • 41
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  • 27
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  • 13
  • 10
  • 8
  • 2
  • 1
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Western Blotting (WB), ELISA
  • Binding Specificity

    • 6
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    AA 310-339

    Cross-Reactivity (Details)

    Expected species reactivity: Primate

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 310-339 from human Rhodopsin was used as the immunogen for this RHO antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the RHO antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    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

    Aliquot the RHO antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    Rhodopsin (RHO)

    Alternative Name

    rho (Rhodopsin)

    Target Type

    Chemical

    Background

    Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.

    UniProt

    P08100

    Pathways

    WNT Signaling, Sensory Perception of Sound, Regulation of G-Protein Coupled Receptor Protein Signaling, Phototransduction
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