Wichtige Dokumente
11835246001
Roche
Apoptotic DNA-Ladder Kit
Synonym(e):
DNA ladder
About This Item
Empfohlene Produkte
Verwendung
sufficient for ≤20 tests
Hersteller/Markenname
Roche
Lagertemp.
20-25°C
Allgemeine Beschreibung
The study of cell death involves characterizing mortality as apoptotic or necrotic. Apoptosis can be characterized by:
- Prelytic, non-random fragmentation of DNA (“ladder” pattern after agarose-gel electrophoresis)1
- Formation of membrane-bound vesicles (or “apoptotic bodies”)
- Cell shrinkage due to a concentration of cytoplasm
Similarly, necrosis (or physiological cell death) is characterized by
- Random digestion of DNA (DNA smear after agarose-gel electrophoresis)
- Swollen organelles and cells, resulting from loss of membrane integrity and cell lysis
- Postlytic DNA fragmentation
As these differences indicate, the classification of cell death can be accomplished through observing cell morphology, or less subjectively, by analyzing genomic DNA. Resolving the DNA on a gel provides a quick and documentable form of data to differentiate between apoptosis and necrosis.
Spezifität
Anwendung
Verpackung
Prinzip
Angaben zur Herstellung
Preparation of Working Solutions
- Add 80 ml ethanol, analysis grade, to Washing Buffer
- Dissolve Positive Control (violet cap) in 400 μl Binding/Lysis Buffer and mix immediately.
- Incubate for 10 minutes at 15 to 25 °C.
EDTA solution (0.5 M)
Dissolve 18.6 g EDTA in 80 ml double dist. water and stir. Adjust pH 8.0 ± 0.1 with 1 M NaOH. EDTA solubilizes at alkaline pH only. After solubilization fill up to 100 ml with double dist. water.
TBE-Buffer
Dissolve 5.4 g Tris, 2.8 g Boric acid in 800 ml double dist. water and add 2 ml
of 0.5 M EDTA solution . Stir until dissolved, final pH 8.0 ± 0.1. Fill up to 1 liter with double dist. water.
Ethidium bromide stock solution
Dissolve 50 mg ethidium bromide in 5 ml double dist. water (ethidium bromide is a mutagen and potential carcinogen; gloves should be worn and care should be taken when handling ethidium bromide solutions).
Alternatively SYBR Green I Nucleic Acid Gel Stain can be used instead of Ethidium bromide.
Loading Buffer (10x)
Dissolve 0.1 g sodium dodecyl sulfate, 25 mg Bromophenol Blue in 7 ml double dist. water and add 3 ml glycerol
Storage conditions (working solution): The positive control can be used for 14 days after preparation, when storing the isolated control DNA at -15 to -25 °C.
Sonstige Hinweise
Rechtliche Hinweise
Nur Kit-Komponenten
- Binding/Lysis Buffer
- Washing Buffer
- Elution Buffer
- Polypropylene Tubes, contain two layers of glass fiber fleece and can hold up to 700 μl sample volume
- Polypropylene Collection Tubes
- Control Apoptotic U937 Cells, lyophilized
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2
Lagerklassenschlüssel
12 - Non Combustible Liquids
WGK
WGK 2
Flammpunkt (°F)
does not flash
Flammpunkt (°C)
does not flash
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Artikel
Cellular apoptosis assays to detect programmed cell death using Annexin V, Caspase and TUNEL DNA fragmentation assays.
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