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CPT2 antibody (AA 33-646)

This anti-CPT2 antibody is a Rabbit Polyclonal antibody detecting CPT2 in WB, ELISA and FACS. Suitable for Human, Mouse and Rat.
Catalog No. ABIN7601357

Quick Overview for CPT2 antibody (AA 33-646) (ABIN7601357)

Target

See all CPT2 Antibodies
CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))

Reactivity

  • 70
  • 36
  • 28
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 65
  • 9
  • 2
Rabbit

Clonality

  • 59
  • 17
Polyclonal

Conjugate

  • 43
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This CPT2 antibody is un-conjugated

Application

  • 55
  • 36
  • 15
  • 11
  • 9
  • 6
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 8
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    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
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    • 1
    • 1
    AA 33-646

    Purpose

    Anti-CPT2/CPT1 Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-CPT2/CPT1 Antibody Picoband® (ABIN7601357). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human CPT2/CPT1 recombinant protein (Position: Q33-D646).

    Isotype

    IgG
  • Application Notes

    "Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    "1. Bonnefont JP, Demaugre F, Prip-Buus C, Saudubray JM, Brivet M, Abadi N, Thuillier L (2000). "Carnitine palmitoyltransferase deficiencies". Mol. Genet. Metab. 68 (4): 424-440. 2. van der Leij FR, Huijkman NC, Boomsma C, Kuipers JR, Bartelds B (2000). "Genomics of the human carnitine acyltransferase genes". Mol. Genet. Metab. 71 (1-2): 139-153. 3. Sigauke E, Rakheja D, Kitson K, Bennett MJ (2003). "Carnitine palmitoyltransferase II deficiency: a clinical, biochemical, and molecular review". Lab. Invest. 83 (11): 1543-1554.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Target

    CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))

    Alternative Name

    CPT2

    Background

    Synonyms: Carnitine O-palmitoyltransferase 2, mitochondrial, Carnitine palmitoyltransferase II, CPT II, CPT2, CPT1

    Tissue Specificity: Expressed mainly in adipose tissues.

    Background: Carnitine O-palmitoyltransferase 2, mitochondrial is an enzyme that in humans is encoded by the CPT2 gene. It is mapped to 1p32.3. The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders.

    Molecular Weight

    74 kDa

    Gene ID

    1376

    UniProt

    P23786

    Pathways

    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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