HiPure Viral Nucleic Aicd Isolation Kit
HiPure Viral Nucleic Aicd Isolation Kit

HiPure Viral Nucleic Aicd Isolati←♥on Kit

BACKGROUND

  Molecular diagnosis and nucleic aci•<≠$d detection have been w§>idely used in thediagnosis of infect✘↕≥ ious or genetic diseases, non-invasive prenatalσ♥Ω× detection,epidemiological investigation, pathoge •nic microorganisms detec$ tion and scientificresearch. Compared w​¥÷φith immunological detection te£¶ ®chniques, nucleic acid detectioncan ob"♦&±tain more sensitive and accurate resul¶φts. The first step in moα™lecular diagnosisinvolves the extraction of nλ‌ucleic acids, which are ♦☆usually bound to organic matterβ≥ α incells, such as histones. The extraction of₹↔ nucleic acids requires first lysing the ceσ$< lls,and then separating t≠""σhe nucleic acids from macromolecular↓€ organic substances (suchas proteins, polysacchar✔"ides, and lipids), while the primary structure of™α the nucleicacids must remain‍÷ intact. The nucleic acid ₩★×≠extraction process currently de$≥'∞pends onqualified profe∑☆✔ssionals to operate. However, with t→✘he rapid development of nucleicacid detection ←£$↔technologies and clinical diagnosis, t™&πhere is an urgent need for asimple and easy-to-u≈∑↓§se method suitable for on-site β↔DNA extraction and d•€♠etection.This method needs to be wid σδely applicable to technical requirements for nu∑¥•cleic acidextraction from primary hospitals,™πλ testing sites and even the ge≥​neral public.

BASIC PRINCIPLES
  This product is based on silica gel colu​γ• mn purification. The sample is lysed, and theDNΩ‌A/RNA is released into the lysis₹™ buffer. After transferring to an adsorption colu‌ ✔mnand filter, DNA/RNA is adso¶₩rbed to the membrane, while the unabsorbed pr ​☆otein isremoved by filtration✘★γ≤ with the solution. After washing away♠©∏ the protein and otherimpurities, DNA/RNA¥≠✘£ is finally eluted by a low-salt bu↕λ♣★ffer to obtain a high-purity‍‌εproduct
PRODOUCT INFORMATION

Applicable specimens: c♥♥★<ell-free/low-cell DNA/RNA sampl‌✔≈es such as clinical or humanbod ↓•y fluids, serum, plasma, soaking flu↕≈≠'id, supernatants from tissue homog§¥☆enate, cellculture supernatant.

Technical principle: silica gel co Ω<lumn purification.

Packing specification: 96 tests/kit, 200 tests/γε×kit.

Storage conditions: 18-25℃ room temperature for 12 mo•₽≈αnths.

PRODOUCT PERFORMANCES

HIGH RECOVERY RATE

silica gel column can recover nucl©☆eic acid molecule₩φ∞s at the picogram level&φ↓↓.

HIGH SENSITIVITY

Recovering viruses DNA/RNA×λ as low as 10 copies.

HIGH QUALITY

Meeting various dow✔←₹nstream applications such as reverse tran ♣$γscription,qPCR,enzyme digestion,blot hyb☆→✔•ridization,etc.

GOOD STABILITY

Stable solution system ensures consistent res↕φ£ults every time.

WIDE APPLICABILITY


Suitable for extract×→εing viral DNA from serum, plasma, milk, cell culΩ'ture supernatant,and variousΩ& cell-free body fluid s✘φα®amples.

FAST

Extraction of multiple samples ₹Ωcan be completed in les±✘€πs than 30 minutes.

OPERATION PROCEDURES