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Luciferase anticorps

L’anticorps Chèvre Polyclonal anti-Luciferase a été validé pour WB et ELISA. Il convient pour détecter Luciferase dans des échantillons de Photinus pyralis. Il y a 2+ publications disponibles.
Rockland
N° du produit ABIN103637
N° du produit (Fournisseur): 100-101-150

Aperçu rapide pour Luciferase anticorps (ABIN103637)

Antigène

Voir toutes Luciferase Anticorps
Luciferase

Reactivité

  • 30
  • 19
  • 8
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Photinus pyralis

Hôte

  • 45
  • 14
  • 9
  • 1
  • 1
Chèvre

Clonalité

  • 42
  • 28
Polyclonal

Conjugué

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  • 10
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  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Luciferase est non-conjugé

Application

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Western Blotting (WB), ELISA
  • N° du produit (Fournisseur)

    100-101-150

    Fournisseur

    Rockland

    Fonction

    Luciferase Antibody

    Réactivité croisée (Details)

    Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-goat serum, purified and partially purified Luciferase [Firefly].

    Attributs du produit

    Synonyms: Goat Anti-Luciferase Antibody, Luciferase Firefly, Goat Anti Luciferase

    Purification

    This product was prepared from monospecific antiserum by a delipidation and defibrination.

    Immunogène

    Immunogen: Luciferase [Firefly]

    Immunogen Type: Native Protein

  • Indications d'application

    Application Note: Anti-Luciferase Antibody has been tested by western blot and is suitable in ELISA. This product can be assayed against 1.0 μg of Luciferase [Firefly] in a standard ELISA using Peroxidase conjugated Affinity Purified anti-Goat IgG [H&L] (Goat) code #611-1302 and (ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) code # ABTS-100 as a substrate for 30 minutes at room temperature.  A working dilution of 1:20,000 to 1:100,000 of the reconstitution concentration is suggested for this product.

    Western Blot Dilution: 1:2,000 - 1:10,000

    ELISA Dilution: 1:20,000 - 1:100,000

    Other: User Optimized

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Reconstitution Volume: 2.0 mL

    Reconstitution Buffer: Restore with deionized water (or equivalent)

    Concentration

    95 mg/mL

    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: None

    Preservative: 0.01 % (w/v) Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store vial at 4° C prior to restoration.   For extended storage aliquot contents and freeze at -20° C or below.  Avoid cycles of freezing and thawing.  Centrifuge product if not completely clear after standing at room temperature.  This product is stable for several weeks at 4° C as an undiluted liquid.  Dilute only prior to immediate use. 

    Date de péremption

    12 months
  • Windahl, Lagerquist, Andersson, Jochems, Kallkopf, Håkansson, Inzunza, Gustafsson, van der Saag, Carlsten, Pettersson, Ohlsson: "Identification of target cells for the genomic effects of estrogens in bone." dans: Endocrinology, Vol. 148, Issue 12, pp. 5688-95, (2008) (PubMed).

    Kenny, Duval, Sammut, Steele, Pritchard, Atherton, Argent, Dimaline, Dockray, Varro: "Increased expression of the urokinase plasminogen activator system by Helicobacter pylori in gastric epithelial cells." dans: American journal of physiology. Gastrointestinal and liver physiology, Vol. 295, Issue 3, pp. G431-41, (2008) (PubMed).

  • Antigène

    Luciferase

    Sujet

    Background: Anti luciferase Antibody recognizes luciferase that is commonly used in biological research as a reporter to assess the transcriptional activity in cells that are transfected with a genetic construct containing the luciferase gene under the control of a promoter of interest. Luciferase can also be used to detect the level of cellular ATP in cell viability assays or for kinase activity assays. Additionally proluminescent molecules that are converted to luciferin upon activity of a particular enzyme can be used to detect enzyme activity in coupled or two-step luciferase assays. Such substrates have been used to detect caspase activity and cytochrome P450 activity, among others.
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