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Septin 9 antibody (AA 536-586)

This Rabbit Polyclonal antibody specifically detects Septin 9 in WB, IP and IF (p). It exhibits reactivity toward Human.
Catalog No. ABIN7453396

Quick Overview for Septin 9 antibody (AA 536-586) (ABIN7453396)

Target

See all Septin 9 (SEPT9) Antibodies
Septin 9 (SEPT9)

Reactivity

  • 29
  • 8
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 25
  • 4
Rabbit

Clonality

  • 28
  • 1
Polyclonal

Conjugate

  • 22
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Septin 9 antibody is un-conjugated

Application

  • 17
  • 11
  • 8
  • 6
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 536-586

    Purpose

    Rabbit anti-Septin 9 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 536 and 586

    Isotype

    IgG
  • Application Notes

    IHC-IF: 1:1,000 - 1:5,000

    IP: 2 - 5 μg/mg lysate

    WB: Not recommended. Use rabbit anti-Septin 9 antibody ABIN7453779.

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 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

    4 °C

    Expiry Date

    12 months
  • Target

    Septin 9 (SEPT9)

    Alternative Name

    Septin 9

    Background

    Background: Septin 9 is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia [taken from NCBI GeneID:10801].

    Gene ID

    10801

    NCBI Accession

    NP_001106963

    UniProt

    Q9UHD8
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