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SATB2 antibody (AA 410-439)

This Rabbit Polyclonal antibody specifically detects SATB2 in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN3032518

Quick Overview for SATB2 antibody (AA 410-439) (ABIN3032518)

Target

See all SATB2 Antibodies
SATB2 (SATB Homeobox 2 (SATB2))

Reactivity

  • 63
  • 35
  • 30
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 55
  • 8
Rabbit

Clonality

  • 41
  • 22
Polyclonal

Conjugate

  • 33
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SATB2 antibody is un-conjugated

Application

  • 43
  • 19
  • 15
  • 13
  • 13
  • 13
  • 8
  • 7
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 16
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 410-439

    Cross-Reactivity (Details)

    Expected species reactivity: Mouse

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 410-439 from the human protein was used as the immunogen for this SATB2 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the SATB2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    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 SATB2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    SATB2 (SATB Homeobox 2 (SATB2))

    Alternative Name

    SATB2

    Background

    This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and mental retardation. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq].

    UniProt

    Q9UPW6
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