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KIF1A antibody (AA 1079-1628)

The Rabbit Polyclonal anti-KIF1A antibody is suitable to detect KIF1A in samples from Mouse, Human and Rat. It has been validated for ELISA, WB and FACS.
Catalog No. ABIN7870017
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for KIF1A antibody (AA 1079-1628) (ABIN7870017)

Target

See all KIF1A Antibodies
KIF1A (Kinesin Family Member 1A (KIF1A))

Reactivity

  • 9
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Mouse, Human, Rat

Host

  • 10
  • 1
Rabbit

Clonality

  • 10
  • 1
Polyclonal

Conjugate

  • 7
  • 2
  • 1
  • 1
This KIF1A antibody is un-conjugated

Application

  • 6
  • 5
  • 2
  • 2
  • 2
  • 1
ELISA, Western Blotting (WB), Flow Cytometry (FACS)
  • Binding Specificity

    • 5
    • 2
    • 1
    • 1
    AA 1079-1628

    Purpose

    KIF1A Antibody

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids H1079-Y1628) was used as the immunogen for the KIF1A antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the KIF1A 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 KIF1A 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

    KIF1A (Kinesin Family Member 1A (KIF1A))

    Alternative Name

    KIF1A

    Background

    Kinesin-like protein KIF1A, also known as axonal transporter of synaptic vesicles or microtubule-based motor KIF1A, is a protein that in humans is encoded by the KIF1A gene. The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described.

    UniProt

    Q12756
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