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CRB1 antibody (AA 301-400) (FITC)

The Rabbit Polyclonal anti-CRB1 antibody has been validated for IF (cc) and IF (p). It is suitable to detect CRB1 in samples from Human.
Catalog No. ABIN6942652

Quick Overview for CRB1 antibody (AA 301-400) (FITC) (ABIN6942652)

Target

See all CRB1 Antibodies
CRB1 (Crumbs Homolog 1 (CRB1))

Reactivity

  • 19
  • 1
  • 1
Human

Host

  • 18
  • 1
Rabbit

Clonality

  • 19
Polyclonal

Conjugate

  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CRB1 antibody is conjugated to FITC

Application

  • 12
  • 12
  • 6
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

    • 14
    • 2
    • 1
    • 1
    AA 301-400

    Cross-Reactivity

    Human

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human CRB1

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    CRB1 (Crumbs Homolog 1 (CRB1))

    Alternative Name

    CRB1

    Background

    Synonyms: CRB1, CRUM1_HUMAN, Protein crumbs homolog 1.

    Background: This gene encodes a protein which is similar to the Drosophila crumbs protein and localizes to the inner segment of mammalian photoreceptors. In Drosophila crumbs localizes to the stalk of the fly photoreceptor and may be a component of the molecular scaffold that controls proper development of polarity in the eye. Mutations in this gene are associated with a severe form of retinitis pigmentosa, RP12, and with Leber congenital amaurosis. Alternate splicing results in multiple transcript variants, some protein coding and some non-protein coding.[provided by RefSeq, Apr 2012]

    Gene ID

    23418

    UniProt

    P82279

    Pathways

    Notch Signaling
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