Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

OCRL antibody (AA 1-901)

The Rabbit Polyclonal anti-OCRL antibody is suitable to detect OCRL in samples from Human. It has been validated for WB, ELISA, IHC (p) and IF.
Catalog No. ABIN7869609
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for OCRL antibody (AA 1-901) (ABIN7869609)

Target

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

Reactivity

  • 22
  • 5
  • 1
  • 1
Human

Host

  • 16
  • 7
Rabbit

Clonality

  • 19
  • 4
Polyclonal

Conjugate

  • 19
  • 2
  • 1
  • 1
This OCRL antibody is un-conjugated

Application

  • 18
  • 13
  • 7
  • 4
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • Binding Specificity

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

    Purpose

    OCRL-1 Antibody

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids M1-D901) was used as the immunogen for the OCRL-1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the OCRL-1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the OCRL-1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

    Alternative Name

    OCRL-1

    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.

    UniProt

    Q01968

    Pathways

    Inositol Metabolic Process
You are here:
Chat with us!