Reagent kit for metagenomic DNA extraction from soil samples "Meta Soil" Raissol

Raissol
metasoil-50

Reagent kit for metagenomic DNA extraction from soil samples "Meta Soil" Raissol is a Raissol reagent product for dna/rna extraction in molecular biology, genetics, diagnostic and research laboratories.

Application area

Used for sample preparation, nucleic acid analysis, PCR/qPCR workflows and sequencing-related projects where applicable.

Sample types

The product is intended for work with pochva.

Advantages of Raissol reagents

  • stable reagent performance and reproducible laboratory results
  • compatibility with common molecular biology protocols
  • convenient workflow for routine and research procedures
  • efficient preparation of biological material for downstream analysis

Key specifications

CategoryDNA and RNA extraction kits;Agrogenetics>>>Agrogenetika - Metagenomnaya DNA;Raissol
ManufacturerRaissol
Primary useDNA/RNA extraction
Sample typePochva

Sample Type: Pochva

Kit contents
Instructions for use
Storage conditions
Required materials and equipment

Kit contents

The kit includes all reagents required for DNA extraction:
1. Lysis buffer - na osnove chaotropic agents i auxiliary components dlya optimal lysis;
2. Binding buffer - dlya povysheniya sorbtsii NA na magnitnykh chastitsakh;
3. Wash buffer 1 - dlya promyvki nucleic acids ot organicheskikh primesey i soley;
4. Wash buffer 2 - dlya promyvki nucleic acids ot organicheskikh primesey i soley;
5. Wash buffer 3 - dlya promyvki nucleic acids ot organicheskikh primesey i soley;
6. Wash buffer 4 - dlya promyvki nucleic acids ot organicheskikh primesey i soley;
7. Elution buffer - dlya elyutsii i khraneniya NA, pH=8,9;
8. Proteinase K - dlya bolee bystrogo i polnogo lizisa;
9. Magnitnye chastitsy - dlya sorbtsii NA.

Instructions for use

Provedenie protsedury extraction metagenomnoy DNA

Lysis
1. V tubes obemom 1,5-2 mL place 100 mg issleduemykh soil samples.
2. K kazhdoy naveske add 400 uL deionizirovannoy vody, isklyuchaya zhidkie pochvy (v t.ch. il).
3. Add k obraztsam 400 uL liziruyushchego bufera i 20 uL Proteinazy K.
4. Intensivno peremeshat tubes on a vortex mixer.
5. Incubate tubes v termostate pri temperature 56℃ v techenie 1-2 chasov, periodicheski peremeshivaya.
6. Sbrosit kapli s pomoshchyu brief centrifugation.
7. Pomestit tubes na led ili v kholodnyy shtativ i inkubirovat v techenie 3 minut. V sluchae otsutstviya okhladitelnykh elementov inkubirovat at room temperature v techenie 10 min until completely cooled smesi.
Sorbtsiya NA
1. Add k smesi 350 uL svyazyvayushchego bufera.
2. Intensivno peremeshat tubes on a vortex mixer, sbrosit kapli s pomoshchyu brief centrifugation.
3. Incubate at room temperature v techenie 5 minut.
4. Centrifuge tubes v techenie 5 minut pri maks. ob/min.
5. Akkuratno, ne zadevaya pellet, perenesti supernatant v novye tubes.
6. Repeat punkty 4-5.
7. Add v tubes 50 uL magnitnykh chastits, mix thoroughly tubes on a vortex mixer.
Rekomendatsiya: add 240 uL izopropanola dlya povysheniya sorbtsii degradirovannoy DNA.
8. Incubate at room temperature v techenie 5 minut, periodicheski peremeshivaya.
9. Sbrosit kapli s pomoshchyu brief centrifugation.
10. Incubate na magnitnom shtative v techenie 5 minut.
11. Akkuratno, ne zadevaya pellet chastits, udalit supernatant.
Nucleic acid washing
1. Add v tubes 500 uL promyvochnogo bufera 1.
2. Intensivno peremeshat tubes on a vortex mixer, sbrosit kapli s pomoshchyu brief centrifugation.
3. Incubate tubes na magnitnom shtative v techenie 2 minut. Akkuratno, ne zadevaya pellet chastits, udalit supernatant.
4. Add v tubes 500 uL promyvochnogo bufera 2.
5. Repeat punkty 2-3.
6. Add v tubes 500 uL promyvochnogo bufera 3.
7. Intensivno peremeshat tubes on a vortex mixer, sbrosit kapli s pomoshchyu brief centrifugation.
8. Incubate tubes na magnitnom shtative v techenie 2 minut. Akkuratno, ne zadevaya pellet chastits, udalit supernatant.
9. Repeat punkty 6-8.
10. Add v tubes 500 uL promyvochnogo bufera 4.
11. Repeat punkty 7-8.
12. Vysushit samples s otkrytymi kryshkami v termostate pri temperature 56-60℃ v techenie 5-10 minut until complete ispareniya promyvochnogo rastvora.
Nucleic acid elution
1. Add v tubes 50-100 uL elyuiruyushchego bufera.
2. Intensivno peremeshat on a vortex mixer, sbrosit kapli s pomoshchyu brief centrifugation.
3. Incubate v termostate pri temperature 56-60℃ v techenie 10 minut, periodicheski peremeshivaya.
4. Sbrosit kapli s pomoshchyu brief centrifugation.
5. Incubate tubes na magnitnom shtative v techenie 3-5 minut.
6. Akkuratno, ne zadevaya chastitsy, perenesti elyuat v novye tubes.

Download the short instruction "MetaSoil" (pdf)

Download the full instruction "MetaSoil" (pdf)

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Storage conditions

Buffers nabora "Meta Soil" can be stored pri temperature ot +4℃ do +25℃ for 12 months from the manufacturer's release date. If a precipitate is present pri minimalnykh temperaturakh khraneniya, warm the solutions to room temperature.
Magnitnye chastitsy can be stored pri temperature ot +4℃ do +25℃ for 12 months from the manufacturer's release date. Pered applicationm suspenziyu chastits neobkhodimo tshchatelno vzbaltyvat do odnorodnogo sostoyaniya.
Enzyme Proteinase K must be stored pri -20℃, shelf life is 12 mesyatsev. A short-term storage temperature increase is allowed (transportation) fermenta Proteinase K ot +4℃ do +25℃ for no more than 5 days.

Required materials and equipment

  1. Microcentrifuge tubes obemom 1,5-2 mL;
  2. Magnitnyy shtativ dlya mikrotsentrifuzhnykh probirok obemom 1,5-2 mL;
  3. Rack for microcentrifuge tubes obemom 1,5-2 mL;
  4. Variable-volume pipettes na 20-200 uL, 100-1000 uL i sootvetstvuyushchie disposable tips;
  5. Vorteks;
  6. Dry block thermostat s vozmozhnostyu podderzhaniya temperaturnogo rezhima v diapazone 25-80ºS dlya probirok obemom 1,5-2 mL;
  7. High-speed microcentrifuge dlya probirok obemom 1,5-2 mL do 13 tys. ob/min;
  8. Cooling rack ili ice maker.