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Recombinant CPT1B antibody

The Rabbit Monoclonal anti-CPT1B antibody (Clone A672) (ABIN7828065) specifically detects CPT1B in WB and IHC. The antibody is reactive with Human samples.
Catalog No. ABIN7828065
$394.68
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for Recombinant CPT1B antibody (ABIN7828065)

Target

See all CPT1B Antibodies
CPT1B (Carnitine Palmitoyltransferase 1B (Muscle) (CPT1B))

Antibody Type

Recombinant Antibody

Reactivity

  • 59
  • 25
  • 20
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 61
  • 1
  • 1
Rabbit

Clonality

  • 62
  • 1
Monoclonal

Conjugate

  • 30
  • 6
  • 5
  • 5
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CPT1B antibody is un-conjugated

Application

  • 56
  • 38
  • 22
  • 13
  • 13
  • 6
  • 5
  • 5
  • 4
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)

Clone

A672
  • Purpose

    Recombinant CPT1B Monoclonal Antibody

    Purification

    Protein A purified

    Immunogen

    Recombinant human CPT1B fragment

    Isotype

    IgG, kappa
  • Application Notes

    WB 1:1000-1:5000,IHC 1:50

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 % protein protectant.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

    Expiry Date

    12 months
  • Target

    CPT1B (Carnitine Palmitoyltransferase 1B (Muscle) (CPT1B))

    Alternative Name

    CPT1B

    Background

    KIAA,KIAA1670,CPT1B,CPT I,CPT1-M,CPTI-M,Carnitine palmitoyltransferase-1 (CPT1), localized to the mitochondrial outer membrane, translocates fatty acids across the mitochondrial membranes and catalyzes the rate-limiting step of β-oxidation. There are three isoforms of this enzyme: CPT1A (liver), CPT1B (muscle), and CPT1C (brain). Deficiency of CPT1A results in an autosomal recessive mitochondrial fatty acid oxidation disorder. Studies have shown that physiological high blood glucose and insulin levels inhibit CPT1B activity in human muscle and therefore divert long-chain fatty acids toward storage in human muscle as triglycerides. Furthermore, mice deficient in CPT1C show less food intake and reduced body weight. These findings suggest that CPT1 may play a role in metabolic syndromes. Cat.No. Product Name Clone No. IF:{{item.impact}} Journal:{{item.journal}} ({{item.year}}) DOI:{{item.doi}} Reactivity:{{item.species}} Sample Type:{{item.sample_type}} Previous {{ page }} Next Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}} Previous {{ page }} Next [

    Molecular Weight

    Calculated MW: 87 kDa

    Observed MW: 87 kDa

    UniProt

    Q92523

    Pathways

    AMPK Signaling, Monocarboxylic Acid Catabolic Process
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