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OCRL antibody (AA 1-901) (Cy3)

The Rabbit Polyclonal anti-OCRL antibody is suitable to detect OCRL in samples from Human. It has been validated for FACS.
Catalog No. ABIN8017917
$570.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for OCRL antibody (AA 1-901) (Cy3) (ABIN8017917)

Target

See all OCRL Antibodies
OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

Reactivity

  • 33
  • 5
  • 1
  • 1
Human

Host

  • 27
  • 7
Rabbit

Clonality

  • 30
  • 4
Polyclonal

Conjugate

  • 21
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This OCRL antibody is conjugated to Cy3

Application

  • 22
  • 17
  • 10
  • 7
  • 5
  • 4
  • 3
  • 1
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

    • 12
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-901

    Purpose

    Anti-OCRL Antibody Cy3 Conjugated

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human OCRL recombinant protein (Position: M1-D901).

    Isotype

    IgG
  • Application Notes

    Flow Cytometry, 1-3 μg/1x106 cells

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    Expiry Date

    12 months
  • Target

    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

    Alternative Name

    OCRL

    Background

    Background: Inositol polyphosphate 5-phosphatase OCRL-1, also known as Lowe oculocerebrorenal syndrome protein, is an enzyme encoded by the OCRL gene located on the X chromosome in humans. This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants.

    Gene Full Name: OCRL inositol polyphosphate-5-phosphatase

    Gene ID

    4952

    UniProt

    Q01968

    Pathways

    Inositol Metabolic Process
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