DMN70
GenElute™ ダイレクトmRNAミニプレップキット
sufficient for 70 purifications
別名:
GenElute™ mRNAキット, GenElute™ダイレクトmRNAミニプレップキット, Gen Elute
詳細
Procedures such as cDNA synthesis, expression profiling and others require separation of mRNA from the vastly more abundant rRNA and tRNA. The GenElute mRNA kits provide convenient procedures for isolating polyadenylated mRNA from previously prepared total RNA or directly from mammalian cells and tissues.
For direct mRNA preparation, cells or tissues are disrupted with SDS/proteinase K digestion to release RNA and eliminate RNases. The kit uses oligo (dT) covalently linked to 1 μm polystyrene beads to capture polyadenylated mRNA by hybridization. The polystyrene beads remain suspended during hybridization, eliminating the need for mixing or rocking, as is common for cellulose or magnetic particles. Polystyrene was also chosen because oligo(dT) polystyrene beads yield cleaner mRNA with fewer stringent washing steps than does the more commonly used oligo(dT) cellulose (2 or 3 wash steps versus 10 or more). With the GenElute kits, mRNA-bead complexes are washed on a microcentrifuge spin filter, and eluted into 10 mM Tris-HCL, pH 7.5.
Up to 107 mammalian cells or 40 mg tissue are lysed and homogenized, either with the filtration columns provided or with a mechanical homogenizer. RNase is eliminated during a 10 minute proteinase K digestion. Sodium chloride is added, and polyadenylated RNA is captured on oligo(dT) polystyrene beads during a 10 minute incubation. For further enrichment, RNA may be released from the beads into fresh lysis solution and recaptured with the original beads. After 3 washes in a spin column, purified mRNA is eluted in 100 μL of 10 mM Tris-HCl, pH 7.4.
The purified mRNA is ready for Northern analysis, reverse transcription and PCR, labeling for arrays, and other common applications.
For direct mRNA preparation, cells or tissues are disrupted with SDS/proteinase K digestion to release RNA and eliminate RNases. The kit uses oligo (dT) covalently linked to 1 μm polystyrene beads to capture polyadenylated mRNA by hybridization. The polystyrene beads remain suspended during hybridization, eliminating the need for mixing or rocking, as is common for cellulose or magnetic particles. Polystyrene was also chosen because oligo(dT) polystyrene beads yield cleaner mRNA with fewer stringent washing steps than does the more commonly used oligo(dT) cellulose (2 or 3 wash steps versus 10 or more). With the GenElute kits, mRNA-bead complexes are washed on a microcentrifuge spin filter, and eluted into 10 mM Tris-HCL, pH 7.5.
Up to 107 mammalian cells or 40 mg tissue are lysed and homogenized, either with the filtration columns provided or with a mechanical homogenizer. RNase is eliminated during a 10 minute proteinase K digestion. Sodium chloride is added, and polyadenylated RNA is captured on oligo(dT) polystyrene beads during a 10 minute incubation. For further enrichment, RNA may be released from the beads into fresh lysis solution and recaptured with the original beads. After 3 washes in a spin column, purified mRNA is eluted in 100 μL of 10 mM Tris-HCl, pH 7.4.
The purified mRNA is ready for Northern analysis, reverse transcription and PCR, labeling for arrays, and other common applications.
The GenElute™ Direct mRNA Miniprep kit provides a convenient format to isolate polyadenylated mRNA directly from mammalian cells and tissues. The direct mRNA isolation procedure is based on that of Badley. Up to 107 mammalian cells or 40 mg tissue are lysed and homogenized, either with the filtration columns provided or with
a mechanical homogenizer. RNase is eliminated during a 10 minute proteinase K digestion. Sodium chloride is added, and polyadenylated RNA is captured on oligo(dT) polystyrene beads during a 10 minute incubation. For further enrichment, RNA may be released from the beads into fresh lysis solution and recaptured with the original beads. After 3 washes in a spin column, purified mRNA is eluted in 100 μl of 10 mM Tris-HCl, pH 7.4.
a mechanical homogenizer. RNase is eliminated during a 10 minute proteinase K digestion. Sodium chloride is added, and polyadenylated RNA is captured on oligo(dT) polystyrene beads during a 10 minute incubation. For further enrichment, RNA may be released from the beads into fresh lysis solution and recaptured with the original beads. After 3 washes in a spin column, purified mRNA is eluted in 100 μl of 10 mM Tris-HCl, pH 7.4.
アプリケーション
GenElute™ Direct mRNA Miniprep Kit has been used to isolate mRNA from various tissues and cells.
The GenElute Direct Kit mRNA kit provides convenient procedures for isolating polyadenylated mRNA from previously prepared total RNA or directly from mammalian cells and tissues.
特徴および利点
- mRNAは10分でoligo(dT)ポリスチレンビ-ズに結合し(Fig. 1)、混和や振盪は不要です。
- total RNAからは40分(Fig. 2)、細胞および組織からは60分(Fig. 3)でPoly (A)+ mRNAを精製します。
- Oligo(dT)ポリスチレンビ-ズを用いているので洗浄回数を減らせます。
- mRNAは10分でoligo(dT)ポリスチレンビ-ズに結合し、混和や振盪は不要です。
- total RNAからは40分、細胞および組織からは60分でPoly (A)+ mRNAを精製します。
- Oligo(dT)ポリスチレンビ-ズを用いているので洗浄回数を減らせます。
法的情報
GenElute is a trademark of Sigma-Aldrich Co. LLC
キットの構成要素のみ
製品番号
詳細
- Collection tube 70 ea
- Elution solution 10 mL
- Filtration columns with tubes 70 ea
- Lysis solution 120 mL
- 5 M NaCl 8 mL
- Oligo(dT)-polystyrene beads 2 mL
- Proteinase K 25 mg
- Spin columns with tubes 70 ea
- 40% Glycerol solution 3 mL
すべて表示 (9)
シグナルワード
Danger
危険有害性情報
危険有害性の分類
Eye Irrit. 2 - Met. Corr. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
8A - Combustible corrosive hazardous materials
適用法令
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Jan Code
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