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Septin 6 antibody (AA 1-434)

The Rabbit Polyclonal anti-Septin 6 antibody is suitable to detect Septin 6 in samples from Human, Mouse and Rat. It has been validated for WB, ELISA, IHC (p) and FACS.
Catalog No. ABIN7869360
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Septin 6 antibody (AA 1-434) (ABIN7869360)

Target

See all Septin 6 (SEPT6) Antibodies
Septin 6 (SEPT6)

Reactivity

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  • 22
  • 12
  • 5
  • 5
  • 5
  • 5
  • 4
  • 4
  • 3
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  • 2
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  • 1
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Human, Mouse, Rat

Host

  • 35
  • 4
  • 3
Rabbit

Clonality

  • 38
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Polyclonal

Conjugate

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  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
  • 1
This Septin 6 antibody is un-conjugated

Application

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  • 3
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  • 2
  • 1
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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

    • 8
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
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    • 1
    AA 1-434

    Purpose

    Septin 6 Antibody / SEPT6

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids M1-E434) was used as the immunogen for the Septin 6 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Septin 6 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 Septin 6 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 6 (SEPT6)

    Alternative Name

    Septin 6

    Background

    Septin-6 is a protein that in humans is encoded by the SEPT6 gene. This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined.

    UniProt

    Q14141
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