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USP14 antibody

The Rabbit Polyclonal anti-USP14 antibody (ABIN7245986) specifically detects USP14 in WB and ELISA. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7245986
$538.80
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 15 Business Days

Quick Overview for USP14 antibody (ABIN7245986)

Target

See all USP14 Antibodies
USP14 (Ubiquitin Specific Peptidase 14 (USP14))

Reactivity

  • 74
  • 20
  • 16
  • 7
  • 2
  • 1
Human, Mouse

Host

  • 64
  • 9
Rabbit

Clonality

  • 46
  • 28
Polyclonal

Conjugate

  • 37
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
This USP14 antibody is un-conjugated

Application

  • 55
  • 28
  • 19
  • 15
  • 15
  • 12
  • 6
  • 6
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human USP14

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.7 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    USP14 (Ubiquitin Specific Peptidase 14 (USP14))

    Alternative Name

    USP14

    Background

    This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases that is a deubiquitinating enzyme (DUB) with His and Cys domains. This protein is located in the cytoplasm and cleaves the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. Mice with a mutation that results in reduced expression of the ortholog of this protein are retarded for growth, develop severe tremors by 2 to 3 weeks of age followed by hindlimb paralysis and death by 6 to 10 weeks of age. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 56 kDa

    UniProt

    P54578
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