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OCRL antibody (AA 150-199)

The Rabbit Polyclonal anti-OCRL antibody (ABIN1453701) specifically detects OCRL in WB and ELISA. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN1453701
$341.00
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Quick Overview for OCRL antibody (AA 150-199) (ABIN1453701)

Target

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

Reactivity

  • 32
  • 4
  • 1
  • 1
Human, Mouse

Host

  • 27
  • 6
Rabbit

Clonality

  • 30
  • 3
Polyclonal

Conjugate

  • 19
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This OCRL antibody is un-conjugated

Application

  • 28
  • 23
  • 18
  • 12
  • 11
  • 4
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 13
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 150-199

    Purpose

    OCRL Antibody

    Specificity

    OCRL Polyclonal Antibody detects endogenous levels of OCRL protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    The antiserum was produced against synthesized peptide derived from human OCRL. AA range:150-199

    Isotype

    IgG
  • Application Notes

    WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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

    Store at -20°C/1 year

    Expiry Date

    12 months
  • Target

    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

    Alternative Name

    OCRL

    Background

    Synonyms: OCRL, INPP5F, OCRL1, Inositol polyphosphate 5-phosphatase OCRL-1, Lowe oculocerebrorenal syndrome protein

    Background: 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. [provided by RefSeq, Jan 2016],

    Gene Name: OCRL

    Protein Name: Inositol polyphosphate 5-phosphatase OCRL-1

    Molecular Weight

    104 kDa

    Gene ID

    4952

    OMIM

    300535

    UniProt

    Q01968

    Pathways

    Inositol Metabolic Process
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