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APOE antibody (AA 95-222)

The Rabbit Polyclonal anti-APOE antibody is suitable to detect APOE in samples from Human. It has been validated for WB, ELISA, IF and FACS.
Catalog No. ABIN7877220
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for APOE antibody (AA 95-222) (ABIN7877220)

Target

See all APOE Antibodies
APOE (Apolipoprotein E (APOE))

Reactivity

  • 130
  • 92
  • 59
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 122
  • 40
  • 11
  • 2
  • 1
Rabbit

Clonality

  • 113
  • 62
Polyclonal

Conjugate

  • 85
  • 19
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  • 3
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  • 3
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  • 1
This APOE antibody is un-conjugated

Application

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  • 2
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Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Binding Specificity

    • 15
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    • 8
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    • 5
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    AA 95-222

    Purpose

    Apolipoprotein E Antibody / APOE

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids E95-Q222) was used as the immunogen for the Apolipoprotein E antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Apolipoprotein E 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 Apolipoprotein E 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

    APOE (Apolipoprotein E (APOE))

    Alternative Name

    Apolipoprotein E

    Background

    Apolipoprotein E is also known as APOE, AD2 or LPG. The protein encoded by this gene is a major apoprotein of the chylomicron. It binds to a specific liver and peripheral cell receptor, and is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. This gene maps to chromosome 19 in a cluster with the related apolipoprotein C1 and C2 genes. Mutations in this gene result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. Alternative splicing results in multiple transcript variants.

    UniProt

    P02649

    Pathways

    Regulation of Cell Size, Lipid Metabolism
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