HiPure Blood DNA ミニカラムキット

$99.00$470.00

送料USD 45 - 米ドル以上は無料 300

DTE は、分子検査のオンライン販売に特化した中国に拠点を置く電子商取引プラットフォームです, エリサ, および関連製品.

  • メーカー: 中国の一流ブランド
  • 配送: 工場から直接FedExで迅速に発送
  • 以内であれば返品または交換が可能です 30 日々
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説明

導入

Blood is a valuable source of DNA for various clinical applications and research studies. しかし, extracting DNA from blood samples presents several challenges:

Safety Concerns:

  • Blood samples can harbor pathogens, posing a risk of infection to researchers and contaminating the lab environment.
  • Traditional methods often involve hazardous chemicals like phenol-chloroform.

DNA Loss:

  • Removing red blood cells, a common pre-treatment step can lead to the loss of desired DNA fractions like viral DNA, circulating DNA, and microbial DNA.

Impurities and Inhibitors:

  • Blood contains various components that can interfere with downstream analyses like PCR and Southern blotting.

New Technology for Improved Blood DNA Extraction:

This product offers a novel approach to address these challenges:

  • Safe and Efficient: The method eliminates the need for red blood cell removal, minimizing infectious waste and potential contamination.
  • Comprehensive DNA Recovery: The protocol allows for the purification of total DNA, including genomic, ミトコンドリア, バイラル, and circulating DNA, providing a more complete picture for analysis.
  • Broad Sample Compatibility: The method effectively purifies DNA from various blood components like whole blood (fresh or frozen), プラズマ, 血清, バフィーコート, などなど.
  • ダウンストリームアプリケーション: The extracted high-quality DNA is suitable for reliable PCR and Southern blotting analyses.

This innovative solution simplifies blood DNA extraction while ensuring safety, efficiency, and comprehensive DNA recovery. It represents a significant advancement for researchers working in various fields like diagnostics, forensics, and medical research.

仕様

特徴仕様
主な機能Isolation total DNA from 200ul Whole Blood
アプリケーションPCR, サザンボルトとウイルスの検出, 等
精製方法Mini スピンカラム
精製技術シリカ技術
加工方法マニュアル (遠心分離または真空)
サンプルの種類Whole Blood (fresh or frozen), 血清, プラズマ, milk, 唾液, and other liquid samples and cultured cells
サンプル量<200μl whole blood or other liquid samples, <5*106 lymphocytes or Culture Cells Non-mammalian animals that have a nucleus in red blood cells (rich in DNA, such as birds and fish): 5~20μl whole blood at a time.
溶出量≥20μl
実行あたりの時間30分以内
カラムあたりの液体搬送量800µl
カラムの結合収量100μg

原理

This product utilizes a silica column-based method for rapid and efficient DNA purification. Here’s a breakdown of the process:

  1. Sample Lysis and Digestion: The sample is treated with a lysate solution and protease to break down cell membranes and degrade proteins. This releases DNA into the solution.
  2. Binding to Silica Membrane: The lysate containing the DNA is transferred to a silica column. The silica membrane in the column specifically binds DNA molecules through favorable interactions. Proteins and other impurities remain unbound.
  3. Washing: Wash buffers are passed through the column, removing unbound proteins and cellular debris that did not adhere to the silica membrane.
  4. Elution: Finally, a low-salt buffer (typically 10 mM トリス, pH 9.0, そして 0.5 mM EDTA) is used to elute the purified DNA from the silica membrane. This buffer disrupts the interaction between DNA and the silica, allowing the purified DNA to be collected in a separate tube.
This method provides a reliable and convenient solution for researchers working in various fields that require purified DNA for analysis, such as PCR, Southern blotting, and next-generation sequencing.

Efficient DNA Purification with Silica Column Technology

This product utilizes a silica column-based method for rapid and efficient DNA purification. Here’s a breakdown of the process:

  1. Sample Lysis and Digestion: The sample is treated with a lysate solution and protease to break down cell membranes and degrade proteins. This releases DNA into the solution.
  2. Binding to Silica Membrane: The lysate containing the DNA is transferred to a silica column. The silica membrane in the column specifically binds DNA molecules through favorable interactions. Proteins and other impurities remain unbound.
  3. Washing: Wash buffers are passed through the column, removing unbound proteins and cellular debris that did not adhere to the silica membrane.
  4. Elution: Finally, a low-salt buffer (typically 10 mM トリス, pH 9.0, そして 0.5 mM EDTA) is used to elute the purified DNA from the silica membrane. This buffer disrupts the interaction between DNA and the silica, allowing the purified DNA to be collected in a separate tube.

利点

  • High-quality DNAmeets a variety of downstream applications, including PCR, qPCR, enzyme digestion, hybridization, 等.
  • 速い – without separation of leukocytes, organic extraction, or ethanol precipitation
  • 単純 – all nucleic acids can be obtained by direct digestion
  • Wide applicability- handle a variety of liquid samples

キット内容

コンテンツD311102D311103
浄化時間50250
HiPure DNA Mini Columns I502 バツ 125
2ml 採取管1005 バツ 100
バッファAL15 ミリリットル60 ミリリットル
Buffer DW130 ミリリットル150 ミリリットル
Buffer GW2*12 ミリリットル50 ミリリットル
プロテイナーゼK24 mg120 mg
プロテアーゼ溶解バッファー1.8 ミリリットル10 ミリリットル
バッファAE15 ミリリットル60 ミリリットル

保管と安定性

最適なパフォーマンスのために:

  • Store Proteinase K at 2-8°C (冷蔵庫) upon arrival.

Acceptable short-term storage:

  • Proteinase K can be stored for up to 12 weeks at room temperature (15-25℃) without affecting its performance.

Remaining kit components:

  • Store all other components of the kit dry at room temperature (15-25℃).
  • They are stable for at least 18 この状況下で数か月.

重要な注意事項:

  • If storing the entire kit at room temperature, ensure buffers are redissolved before use and always warm all buffers to room temperature before using them.

追加情報

重さ0.7 kg
サイズ

HiPure Blood DNA ミニキット 50 準備, HiPure Blood DNA ミニキット 250 準備

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