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KIF5A antibody (Isoform 5)

The Rabbit Polyclonal anti-KIF5A antibody is suitable to detect KIF5A in samples from Human, Mouse and Rat. It has been validated for WB, ELISA and FACS.
Catalog No. ABIN7874433
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for KIF5A antibody (Isoform 5) (ABIN7874433)

Target

See all KIF5A Antibodies
KIF5A (Kinesin Family Member 5A (KIF5A))

Reactivity

  • 20
  • 15
  • 11
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

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  • 3
  • 1
Rabbit

Clonality

  • 27
  • 3
Polyclonal

Conjugate

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  • 2
This KIF5A antibody is un-conjugated

Application

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  • 8
  • 8
  • 3
  • 3
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  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 374-1032, Isoform 5

    Purpose

    KIF5A Antibody / Kinesin heavy chain isoform 5A

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids E374-S1032) was used as the immunogen for the KIF5A antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the KIF5A 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 KIF5A 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

    KIF5A (Kinesin Family Member 5A (KIF5A))

    Alternative Name

    KIF5A

    Background

    Kinesin heavy chain isoform 5A is a protein that in humans is encoded by the KIF5A gene. This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10.

    UniProt

    Q12840
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