Sanshibio Agarose

$58.00

배송비(USD) 45 - USD 이상 무료 300

DTE는 분자 테스트 온라인 판매를 전문으로 하는 중국 기반의 전자상거래 플랫폼입니다., 엘리사, 및 관련 제품.

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설명

제품소개

  • Support Material: Agarose serves as a common support material in gel electrophoresis.
  • Purity Impact: The purity of agarose directly influences the resolution of DNA bands and the clarity of electrophoresis results.
  • 준비: 아가로스, a high-purity form of agar, is typically prepared as a gel with concentrations ranging from 0.5% 에게 2%.
  • 응용: Agarose gel electrophoresis is utilized for the separation and identification of nucleic acids, including DNA profiling and DNA restriction enzyme mapping.
  • Visualization: Nucleic acid fluorescent dyes are added to the gel, and DNA bands are visualized using a gel imaging scanner post-electrophoresis.

상품 내용:

구성요소DA003-02(100g)
아가로스100g

Quality Control:

Parameter사양
Gel Strength (1% 젤라틴)> 1200g/cm²
Electroendosmosis (EEO)< 0.15
황산염≤ 0.15%
겔 온도 (1.5% 젤라틴)35-37℃
Melting Temperature (1.5% 젤라틴)87-89℃
수분≤ 10%

Absence of Nucleases.

Usage Instructions:

  • Depending on the size of the target nucleic acid fragments and the type of electrophoresis buffer, determine the required agarose concentration:
Agarose concentrationIdeal linear resolution range(bp)
1× TAE1× TBE
0.6%1200-150001200-12000
0.8%1000-100001000-12000
1.0%200-10000100-10000
1.2%100-8000100-5000
1.5%100-500050-3000
2.0%50-300050-3000
2.5%50-300050-2000
  • 아가로스 젤 준비 (Horizontal Gel Electrophoresis Example):
  • Based on the amount of gel needed and the desired agarose concentration, 전기영동 완충액의 적정량을 측정합니다. (TAE 또는 TBE) 그리고 삼각플라스크에 부어주세요..

메모: The buffer used for gel preparation should be the same as the electrophoresis buffer.

  • Accurately weigh the agarose and carefully add it to the triangular flask. Cover the flask opening with parchment paper and heat it in a microwave oven to dissolve the agarose. Heat the solution until it boils, then wearing heat-resistant gloves, gently swirl the flask. Repeat this process several times until the agarose is completely dissolved.

메모: Use multiple short boiling steps during the agarose dissolution to avoid overheating and boiling over. Ensure the agarose is fully dissolved to avoid blurry electrophoresis results.

  • Add nucleic acid dye to the fully dissolved agarose solution.
  • Pour the agarose solution into the gel mold, then insert the comb at the appropriate position. The gel thickness is usually between 3-5mm.
  • Let the gel solidify at room temperature (약 30 분까지 1 시간) and then place it in the electrophoresis apparatus for electrophoresis.

지침:

  1. Beware of boiling during the agarose dissolution process to prevent scalding.
  2. DA003-01 is a domestic proprietary brand, and DA003-02 is an imported reagent.
  3. Please wear gloves, especially when using fluorescent dyes with carcinogenic properties (such as ethidium bromide) for gel nucleic acid staining.
  4. If the prepared gel is not used immediately, store it submerged in electrophoresis buffer (TAE 또는 TBE) 에게 avoid gel drying out.

참고용 Solarbio 제품에 대한 고객 리뷰

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