BaculoDirect™ C-Term Expression Kit
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Invitrogen™

BaculoDirect™ C-Term Expression Kit

BaculoDirect™ Baculovirus Expression Systemは、昆虫細胞における高レベルのタンパク質発現のための強力で汎用性の高い真核生物システムです。Gateway™テクノロジーとバキュロウイルス発現を組み合わせることで、BaculoDirect Systemで組換えバキュロウイルスを迅速かつ簡単に生成できます。ワークフロー:BaculoDirect™ Linear詳細を見る
製品番号(カタログ番号)数量
125620135 transfections
製品番号(カタログ番号) 12562013
価格(JPY)
272,100
Each
お問い合わせください ›
数量:
5 transfections
BaculoDirect™ Baculovirus Expression Systemは、昆虫細胞における高レベルのタンパク質発現のための強力で汎用性の高い真核生物システムです。Gateway™テクノロジーとバキュロウイルス発現を組み合わせることで、BaculoDirect Systemで組換えバキュロウイルスを迅速かつ簡単に生成できます。

ワークフロー:
BaculoDirect™ Linear DNA(バキュロウイルスゲノム)は、Gatewayエントリークローンで迅速かつ効率的に組換えを行うために、attR部位を含めるように設計されています。目的の遺伝子は、シンプルな1時間のLR反応を使用して、エントリークローンからBaculoDirect Linear DNAに組換えられます(図1)。結果として得られる反応ミックスには、目的遺伝子を持つ組換えバキュロウイルスが含まれ、昆虫細胞のトランスフェクションに使用されます。細菌を形質転換して大規模なバクミドを単離したり、または転送ベクターとリニアバキュロウイルスDNAの昆虫細胞への相互トランスフェクションを行ったりする必要がなくなります。その結果、ハンズオン時間が大幅に短縮されます。浄化されたバキュロウイルスは1週間以内に単離できます。

Gateway線形DNA
BaculoDirect Linear DNAは、Gatewayエントリークローンでの迅速なクローニングと、その後のSf9またはSf21昆虫細胞における発現のために設計されています。Linear DNAの特徴:

•高レベルでの発現用の強力なポリヘドリンプロモーター
• 任意のattL側Gatewayエントリーベクターを使用した効率的な組換えのためのR部位
• ガンシクロビルを使用したネガティブ選択のためのTK遺伝子
• 抗V5抗体での検出およびニッケルキレート樹脂での浄化ためのC末端V5-Hisタグ(BaculoDirect™ C-Term Expression Kit)またはN末端V5-Hisタグ(BaculoDirect™ N-Term Expression Kit)
• V5-Hisタグの除去とそれに続く浄化のためのTEVプロテアーゼ切断部位(BaculoDirect N-Termic Expression Kit)
• 純粋なバキュロウイルスストックが確実に生成されるようにするLacZ遺伝子。これは、LR組換え反応後、目的の遺伝子に置き換えられます。

必要な追加の原材料、個別に使用可能:Gatewayエントリークローン。

アプリケーションに最適なGatewayエントリーベクターの選択ガイドについては、www.thermofisher.com/Gatewayをご覧ください。

研究用にのみ使用できます。診断用には使用いただけません。
仕様
製品タイプExpression Kit
数量5 transfections
ベクターBaculoDirectベクター
クローニング法Gateway™
製品ラインBaculoDirect、Gateway, Gateway
プロモーターポリヘドリン
タンパク質タグHisタグ(6x)、V5エピトープタグ, V5 Epitope Tag
Unit SizeEach
組成および保存条件
BaculoDirect expression kitsには、BaculoDirect Linear DNAの0.3 µgのバイアル5本、125 µLのCellfectinトランスフェクション試薬、凍結されたSf9細胞、Gateway LRクロナーゼ酵素ミックス、IBCO Unsupplemented Grace's Insect Medium、およびガンシクロビルが含まれます。

BaculoDirect Linear DNA、Cellfectin試薬、Grace's MedIumを+4℃で保管してください。LRクロナーゼミックスは-80℃で保管してください。Sf9細胞を液体窒素に保管してください。すべての成分は、適切に保管した場合、6ヶ月間安定しています。

よくあるご質問(FAQ)

I cannot grow this white colony in liquid culture. What should I do?

The concentration of gentamicin might be too high. Try lowering the amount to 5 µg/mL and try adding more of the colony to the culture medium.

What has happened when I see blue colonies? How about colonies which are blue in the center and white on the edges?

In the case of a blue colony, the E. coli has the bacmid and the plasmid in it, allowing the cells to survive the selection process. However, because the transposition has not occurred, the LacZ gene is not disrupted. For bulls-eye colonies, this indicates that the transposition took place when the colony was growing. Re-streaking for an isolated clone from the white portion of the mixed colony should yield some colonies where transposition occurred.

I'm getting mostly white/wild-type plaques instead of blue/recombinant plaques. What am I doing wrong?

This is typically an indication of poor homologous recombination. Check the plasmid/linear DNA ratio you used. If there are some blue plaques, however, expand those viruses and check for their protein. In our experience, they are correct, even if they were in relatively low abundance.

I've infected my cells and see large polyhedra in one cell and smaller polyhedra (more numerous) in a neighboring cell. Is this normal?

Yes, cells are infected with wild-type virus individually and will develop polyhedra at different rates until all the cells in the flask are infected. The polyhedra in cells will form in approximately 3-4 days, differing in size and number until they reach their maximum capacity and burst the cell, releasing tiny particles of virus into the medium.

I'm worried that I am not getting plaques. How many days does it take to see plaques and what size are they typically?

Normally, very small white dots show up about 5-7 days and 1 mm plaques show up around day 10. Plaques can vary in size from 1 mm to 4 mm.

引用および参考文献 (9)

引用および参考文献
Abstract
Functional characterization of five novel CYP2C8 variants, G171S, R186X, R186G, K247R, and K383N, found in a Japanese population.
Authors:Hichiya H, Tanaka-Kagawa T, Soyama A, Jinno H, Koyano S, Katori N, Matsushima E, Uchiyama S, Tokunaga H, Kimura H, Minami N, Katoh M, Sugai K, Goto Y, Tamura T, Yamamoto N, Ohe Y, Kunitoh H, Nokihara H, Yoshida T, Minami H, Saijo N, Ando M, Ozawa S, Saito Y, Sawada J,
Journal:Drug Metab Dispos
PubMed ID:15716363
Cytochrome P450 2C8 is one of the primary enzymes responsible for the metabolism of a wide range of drugs such as paclitaxel, cerivastatin, and amiodarone. We have sequenced the CYP2C8 gene from 201 Japanese subjects and found five novel nonsynonymous single nucleotide polymorphisms (SNPs): 511G>A (G171S), 556C>T (R186X; X represents the translational stop ... More
Analysis of the large inactive P-TEFb complex indicates that it contains one 7SK molecule, a dimer of HEXIM1 or HEXIM2, and two P-TEFb molecules containing Cdk9 phosphorylated at threonine 186.
Authors:Li Q, Price JP, Byers SA, Cheng D, Peng J, Price DH,
Journal:J Biol Chem
PubMed ID:15965233
'Positive transcription elongation factor b (P-TEFb) regulates eukaryotic gene expression at the level of elongation, and is itself controlled by the reversible association of 7SK RNA and an RNA binding protein, HEXIM1 or HEXIM2. To further understand how P-TEFb is regulated, we analyzed the stoichiometry of all the known components ... More
HEXIM2, a HEXIM1-related protein, regulates positive transcription elongation factor b through association with 7SK.
Authors:Byers SA, Price JP, Cooper JJ, Li Q, Price DH,
Journal:J Biol Chem
PubMed ID:15713662
'The kinase activity of positive transcription elongation factor b (P-TEFb), composed of cyclin-dependent kinase 9 and cyclin T1 or T2, is required for the transition of RNA polymerase II into productive elongation. P-TEFb activity has been shown to be negatively regulated by association with the small nuclear RNA 7SK and ... More
Replication-dependent destruction of Cdt1 limits DNA replication to a single round per cell cycle in Xenopus egg extracts.
Authors:Arias EE, Walter JC,
Journal:Genes Dev
PubMed ID:15598982
'In eukaryotes, prereplication complexes (pre-RCs) containing ORC, Cdc6, Cdt1, and MCM2-7 are assembled on chromatin in the G1 phase. In S phase, when DNA replication initiates, pre-RCs are disassembled, and new pre-RC assembly is restricted until the following G1 period. As a result, DNA replication is limited to a single ... More
Characterization of Aplysia enticin and temptin, two novel water-borne protein pheromones that act in concert with attractin to stimulate mate attraction.
Authors:Cummins SF, Nichols AE, Amare A, Hummon AB, Sweedler JV, Nagle GT,
Journal:J Biol Chem
PubMed ID:15054104
'Mate attraction in Aplysia involves a long-distance water-borne signal (attractin) that is released during egg laying. Other pheromones are predicted to be released during egg laying that act in concert with albumen gland attractin to stimulate attraction, but their identities are unknown. To identify other candidate water-borne pheromones, we employed ... More