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EGR2 antibody (AA 200-300)

This anti-EGR2 antibody is a Rabbit Polyclonal antibody detecting EGR2 in WB. Suitable for Human.
Catalog No. ABIN7266888

Quick Overview for EGR2 antibody (AA 200-300) (ABIN7266888)

Target

See all EGR2 Antibodies
EGR2 (Early Growth Response 2 (EGR2))

Reactivity

  • 67
  • 45
  • 27
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 65
  • 5
  • 1
Rabbit

Clonality

  • 55
  • 16
Polyclonal

Conjugate

  • 38
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EGR2 antibody is un-conjugated

Application

  • 54
  • 24
  • 13
  • 13
  • 9
  • 9
  • 6
  • 6
  • 4
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 7
    • 4
    • 3
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    • 2
    • 2
    • 2
    • 2
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    • 1
    • 1
    • 1
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    AA 200-300

    Purpose

    EGR2 Rabbit pAb

    Sequence

    LAYPPPPSYP SPKPATDPGL FPMIPDYPGF FPSQCQRDLH GTAGPDRKPF PCPLDTLRVP PPLTPLSTIR NFTLGGPSAG VTGPGASGGS EGPRLPGSSS A

    Cross-Reactivity

    Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic peptide corresponding to a sequence within amino acids 200-300 of human EGR2 (NP_000390.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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. Avoid freeze / thaw cycles.
  • Target

    EGR2 (Early Growth Response 2 (EGR2))

    Alternative Name

    EGR2

    Background

    The protein encoded by this gene is a transcription factor with three tandem C2H2-type zinc fingers. Defects in this gene are associated with Charcot-Marie-Tooth disease type 1D (CMT1D), Charcot-Marie-Tooth disease type 4E (CMT4E), and with Dejerine-Sottas syndrome (DSS). Multiple transcript variants encoding two different isoforms have been found for this gene.,EGR2,AT591,CMT1D,CMT4E,KROX20,Epigenetics & Nuclear Signaling,Transcription Factors,Neuroscience,Neurodegenerative Diseases,EGR2

    Molecular Weight

    44kDa/50kDa

    Gene ID

    1959

    UniProt

    P11161
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