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TUBB3 antibody (AA 383-412)

This anti-TUBB3 antibody is a Rabbit Polyclonal antibody detecting TUBB3 in WB and IHC (p). Suitable for Human, Mouse and Rat.
Catalog No. ABIN5647331

Quick Overview for TUBB3 antibody (AA 383-412) (ABIN5647331)

Target

See all TUBB3 Antibodies
TUBB3 (Tubulin, beta 3 (TUBB3))

Reactivity

  • 157
  • 75
  • 68
  • 21
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  • 8
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  • 4
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Human, Mouse, Rat

Host

  • 91
  • 74
  • 4
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Rabbit

Clonality

  • 94
  • 77
Polyclonal

Conjugate

  • 92
  • 14
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  • 3
  • 3
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  • 3
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  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TUBB3 antibody is un-conjugated

Application

  • 139
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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 28
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    AA 383-412

    Purification

    Antigen affinity purified

    Immunogen

    Amino acids 383-412 (EQFTAMFRRKAFLHWYTGEGMDEMEFTEAE-human) were used as the immunogen for the Beta III Tubulin antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Beta III Tubulin antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,Immunohistochemistry (FFPE): 1-2 μg/mL

    Restrictions

    For Research Use only
  • Buffer

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

    Storage

    -20 °C

    Storage Comment

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

    TUBB3 (Tubulin, beta 3 (TUBB3))

    Alternative Name

    Tubulin beta 3 / TUBB3

    Background

    Tubulin beta-3 chain is a protein that in humans is encoded by the TUBB3 gene. This gene encodes a class III member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. This protein is primarily expressed in neurons and may be involved in neurogenesis and axon guidance and maintenance. Mutations in this gene are the cause of congenital fibrosis of the extraocular muscles type 3. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 6.

    UniProt

    Q13509

    Pathways

    Microtubule Dynamics, M Phase
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