Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Septin 9 antibody (AA 15-282)

This Rabbit Polyclonal antibody specifically detects Septin 9 in WB, IF, ELISA, FACS and IHC (p). It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7870787
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Septin 9 antibody (AA 15-282) (ABIN7870787)

Target

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

Reactivity

  • 33
  • 9
  • 7
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse

Host

  • 29
  • 4
Rabbit

Clonality

  • 32
  • 1
Polyclonal

Conjugate

  • 26
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Septin 9 antibody is un-conjugated

Application

  • 20
  • 11
  • 8
  • 7
  • 6
  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 15-282

    Purpose

    SEPT9 Antibody / Septin 9

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids R15-D282) was used as the immunogen for the SEPT9 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the SEPT9 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the SEPT9 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    Septin 9 (SEPT9)

    Alternative Name

    SEPT9

    Background

    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.

    UniProt

    Q9UHD8
You are here:
Chat with us!