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AFF2 antibody (AA 886-912)

The Rabbit Polyclonal anti-AFF2 antibody has been validated for WB. It is suitable to detect AFF2 in samples from Human.
Catalog No. ABIN1538678

Quick Overview for AFF2 antibody (AA 886-912) (ABIN1538678)

Target

See all AFF2 Antibodies
AFF2 (AF4/FMR2 Family, Member 2 (AFF2))

Reactivity

  • 41
  • 10
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 40
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Rabbit

Clonality

  • 40
  • 1
Polyclonal

Conjugate

  • 11
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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This AFF2 antibody is un-conjugated

Application

  • 30
  • 17
  • 13
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  • 1
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Western Blotting (WB)

Clone

RB24533
  • Binding Specificity

    • 15
    • 6
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    • 1
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    AA 886-912

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This AFF2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 886-912 amino acids from the Central region of human AFF2.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    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

    AFF2 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    AFF2 (AF4/FMR2 Family, Member 2 (AFF2))

    Alternative Name

    AFF2

    Background

    This gene encodes a putative transcriptional activator that is a member of the AF4FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked mental retardation. Alternate splicing results in multiple transcript variants.

    Molecular Weight

    144771

    Gene ID

    2334

    NCBI Accession

    NP_001162593, NP_001162594, NP_001162595, NP_001162596, NP_001164099, NP_002016

    UniProt

    P51816
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