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TUBB3 antibody

The Rabbit Polyclonal anti-TUBB3 antibody has been validated for WB and IF. It is suitable to detect TUBB3 in samples from Human, Mouse and Rat.
Catalog No. ABIN7259556
-15% Promotion 2026
$642.60
$756.00
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Quick Overview for TUBB3 antibody (ABIN7259556)

Target

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

Reactivity

  • 176
  • 101
  • 95
  • 21
  • 9
  • 8
  • 6
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 112
  • 70
  • 4
  • 1
  • 1
Rabbit

Clonality

  • 115
  • 73
Polyclonal

Conjugate

  • 83
  • 13
  • 13
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 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

  • 155
  • 92
  • 57
  • 54
  • 41
  • 35
  • 35
  • 31
  • 20
  • 15
  • 15
  • 14
  • 6
  • 5
  • 4
  • 4
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human TUBB3.

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    TUBB3 (Tubulin, beta 3 (TUBB3))

    Alternative Name

    TUBB3

    Background

    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.

    Molecular Weight

    Observed_MW: 55 kDa

    Calculated_MW: 42 kDa/50 kDa

    Gene ID

    10381

    UniProt

    Q13509

    Pathways

    Microtubule Dynamics, M Phase
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