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GFAP antibody (pSer8)

This Rabbit Polyclonal antibody specifically detects GFAP in ELISA and DB. It exhibits reactivity toward Human.
Catalog No. ABIN3028681

Quick Overview for GFAP antibody (pSer8) (ABIN3028681)

Target

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

Reactivity

  • 346
  • 223
  • 221
  • 76
  • 73
  • 56
  • 54
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  • 6
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  • 2
  • 1
  • 1
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  • 1
Human

Host

  • 229
  • 197
  • 13
  • 8
  • 2
  • 2
  • 2
Rabbit

Clonality

  • 242
  • 208
  • 2
Polyclonal

Conjugate

  • 226
  • 39
  • 25
  • 17
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  • 3
  • 3
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  • 2
  • 1
  • 1
  • 1
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  • 1
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This GFAP antibody is un-conjugated

Application

  • 342
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  • 110
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  • 89
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  • 43
  • 33
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  • 1
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ELISA, Dot Blot (DB)
  • Binding Specificity

    • 34
    • 25
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    • 16
    • 16
    • 12
    • 12
    • 10
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    • 1
    • 1
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    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    pSer8

    Purification

    Antigen affinity purified

    Immunogen

    This phospho-GFAP antibody was produced from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding pS8 of human GFAP.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the phospho-GFAP antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Dot blot: 1:500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS pH 7.4 with 0.09 % 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

    Aliquot the phospho-GFAP antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 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.

    UniProt

    P14136
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