Conjunto de ADNasa

De$362.00

Envío USD 45 - Gratis sobre USD 300

Kit DNase I libre de RNasa con búfer de digestión

DTE es una plataforma de comercio electrónico con sede en China que se especializa en ventas en línea de pruebas moleculares., ELISA, y productos relacionados.

  • Fabricante: Marcas chinas líderes
  • Envío: Envío acelerado de FedEx directamente desde las fábricas
  • Elegible para devolución o reemplazo dentro de 30 días
  • Métodos de pago: PayPal seguro o tarjeta de crédito.

Descripción

Nota:Este producto debe empacarse con bolsas de hielo y enviarse a través de FedEx o UPS..
It will arrive within 7–10 days. Los gastos de envío están incluidos en el precio del producto..

Introducción

Bovine Pancreatic Deoxyribonuclease (ADNasa I)

  1. Nature and Function:
    • DNase I is an endonuclease enzyme extracted from bovine pancreas.
    • It primarily acts on DNA, cleaving the phosphodiester bonds, especially those adjacent to a pyrimidine nucleoside.
    • The cleavage results in oligonucleotides that terminate with a phosphate group at the 5end and a hydroxyl group at the 3′ fin.
  2. Optimal Conditions and Stabilization:
    • The optimum pH for DNase I activity is 7.8.
    • It requires divalent metal ions for activation; common activators include magnesium and calcium ions.
    • 5 mM calcium ions are particularly used to stabilize DNase I, protecting it from degradation by proteases.
  3. Inhibition:
    • DNase I activity can be inhibited by chelating agents such as EDTA, which bind and remove divalent cations essential for its activity.
    • Dodecil sulfato de sodio (Ficha de datos de seguridad (MSDS)) also inhibits its activity, likely through interference with the enzyme’s interaction with DNA.
  4. Purification:
    • The enzyme is purified through chromatographic techniques to remove contaminants, particularly other hydrolases.

RNase Free DNase I Set (For RNA Purification)

  1. Objetivo:
    • This kit is designed for the removal of DNA from RNA preparations in column or magnetic bead-based extracción de ARN protocols.
  2. Procedimiento:
    • Biological samples are initially lysed, and ethanol is added to optimize conditions for RNA binding to the column or magnetic beads.
    • After binding, the sample undergoes a wash step to remove impurities.
  3. DNA Digestion:
    • ADNasa I, along with a specific buffer, is applied to the RNA-bound membrane or beads.
    • The mixture is incubated at room temperature (25-37 °C) for about 15 minutos, allowing DNase I to digest and remove any DNA present.
  4. Post-Digestion Processing:
    • Following digestion, the column, or beads are washed to remove DNase and the degraded DNA fragments.
    • Finalmente, RNA is eluted using DEPC-treated water to prevent any RNAse contamination.

Detalles

Especificaciones

Características Especificaciones
Peso molecular 32kda
Isoelectric point 8.9
pH range 4.0–10.0
Actividad específica 10 kunitz units/μl


Ventajas

  • Pure natural protein, from bovine pancreas
  • High activity and purity, >10 kunitz units/μl
  • High cost performance
  • Completely remove RNase contamination
  • Ready to use liquid type
  • Ultra-high dosage (10μl/time,100μ/time) to remove more genomic DNA

Información sobre pedidos

Contenido C12133 C12134
RNase-Free DNase I (10 units/μl)

Plus DNase Buffer

500 preparativos (Plus 60 ml DNase Buffer) 5000 preparativos (Plus 600 ml DNase Buffer)

Almacenamiento y estabilidad

Magen RNase-Free DNase I is stable for up to 1 year after delivery when stored at -20 °C.

Información adicional

Peso 0.75 kg
tamaño

Conjunto de ADNasa 500 preparativos, Conjunto de ADNasa 10 X 500 preparativos

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