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GFAP antibody (N-Term)

The Rabbit Polyclonal anti-GFAP antibody (Clone RB2895) (ABIN388755) specifically detects GFAP in WB. The antibody is reactive with Human samples.
Catalog No. ABIN388755
$451.00
Plus shipping costs $50.00
Shipping to: United States
Delivery in 10 to 12 Business Days

Quick Overview for GFAP antibody (N-Term) (ABIN388755)

Target

See all GFAP Antibodies
GFAP (Glial Fibrillary Acidic Protein (GFAP))

Reactivity

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  • 73
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  • 53
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Human

Host

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  • 14
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  • 2
  • 2
Rabbit

Clonality

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  • 197
  • 1
Polyclonal

Conjugate

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This GFAP antibody is un-conjugated

Application

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Western Blotting (WB)

Clone

RB2895
  • Binding Specificity

    • 46
    • 24
    • 21
    • 16
    • 11
    • 10
    • 10
    • 8
    • 8
    • 8
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    • 7
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    • 1
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    • 1
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    AA 10-40, N-Term

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    Immunogen

    This GFAP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 10-40 amino acids from the N-terminal region of human GFAP.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. WB: 1:8000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    GFAP (Glial Fibrillary Acidic Protein (GFAP))

    Alternative Name

    GFAP

    Background

    GFAP is one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system.

    Molecular Weight

    49880

    Gene ID

    2670

    NCBI Accession

    NP_001124491, NP_001229305, NP_002046

    UniProt

    P14136
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