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Septin 9 antibody

This anti-Septin 9 antibody is a Rabbit Polyclonal antibody detecting Septin 9 in WB. Suitable for Human.
Catalog No. ABIN7467359

Quick Overview for Septin 9 antibody (ABIN7467359)

Target

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

Reactivity

  • 30
  • 8
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 26
  • 4
Rabbit

Clonality

  • 29
  • 1
Polyclonal

Conjugate

  • 23
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Septin 9 antibody is un-conjugated

Application

  • 17
  • 11
  • 8
  • 6
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Cross-Reactivity

    Human, Mouse

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human SEPT9. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:1000-1:10000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: Raji , Mouse liver

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.03 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    Septin 9 (SEPT9)

    Alternative Name

    septin 9

    Background

    Septin 9 , AF17q25 , MSF , MSF1 , NAPB , PNUTL4 , SINT1 , SeptD1,This gene 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. Multiple alternatively spliced transcript variants encoding different isoforms have been described.

    Molecular Weight

    65 kDa

    Gene ID

    10801

    UniProt

    Q9UHD8
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