pIZ/V5-His Vector Kit
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Invitrogen™

pIZ/V5-His Vector Kit

InsectSelect™ Kitには、目的のさまざまな遺伝子の高レベル発現用のpIZ/V5-Hisベクターが含まれています。この非常に小さなベクターには、昆虫細胞における組換えタンパク質の発現、分析、および検出を容易にするいくつかの機能があります:• 構成的発現用のOpIE2プロモーター• 安定的にトランスフェクションされた細胞株を迅速に選択するためのゼオシン耐性遺伝子• Invitrogenの抗V5抗体での検出とニッケルキレート樹脂による簡単な浄化のためのC末端V5エピトープおよびポリヒスチジン詳細を見る
製品番号(カタログ番号)数量
V800001
または、製品番号V8000-01
1 kit
製品番号(カタログ番号) V800001
または、製品番号V8000-01
価格(JPY)
143,900
1 kit
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数量:
1 kit
InsectSelect™ Kitには、目的のさまざまな遺伝子の高レベル発現用のpIZ/V5-Hisベクターが含まれています。この非常に小さなベクターには、昆虫細胞における組換えタンパク質の発現、分析、および検出を容易にするいくつかの機能があります:

• 構成的発現用のOpIE2プロモーター
• 安定的にトランスフェクションされた細胞株を迅速に選択するためのゼオシン耐性遺伝子
• Invitrogenの抗V5抗体での検出とニッケルキレート樹脂による簡単な浄化のためのC末端V5エピトープおよびポリヒスチジン(6xHis)配列
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
製品タイプ昆虫細胞発現ベクター
タンパク質のタグ位置(遺伝子に対して)C-末端
数量1 kit
ベクターpIZ
クローニング法制限酵素/MCS
製品ラインInsectSelect
プロモーターOplE2
タンパク質タグHisタグ(6x)、V5エピトープタグ, V5 Epitope Tag
Unit Size1 kit
組成および保存条件
InsectSelect™ Kitには、それぞれ20 μgの超らせん型の凍結乾燥されたpIZ/V5-HisおよびpIZ/V5-His/CAT、2 μgの凍結乾燥されたOpIE2逆シーケンシングプライマー、1 gのZeocin™、Cellfectin™試薬、および選択した昆虫細胞株用の1 Lの培地が含まれています。Sf9細胞にはGIBCO™ Grace's Insect Mediaが付属し、High Five™細胞にはGIBCO™ Express Five™ Serum-Free Mediumが付属しています。pIZ/V5-His Vector Kitには、上記の発現ベクターおよびプライマーのみが含まれています。凍結した昆虫細胞を液体窒素中に保管してください。培地およびCellfectin™試薬を+4℃で保管してください。その他のすべての試薬を-20℃で保管してください。すべての試薬は、適切な保管条件であれば、6カ月間安定していることが保証されています。

よくあるご質問(FAQ)

Do I need to include a Kozak sequence for expression of recombinant proteins in insect cells?

While the importance of a Kozak consensus sequence in translation initiation has been demonstrated in mammalian cells, there seems to be some debate as to whether the Kozak rules are as stringent in insect cells. The only way to determine its importance would be a direct comparison of expression of the same protein from different initiation sequences. Even then, the rules for optimal expression of one protein may not hold for another. Here are two references which indicate that a Kozak consensus sequence does not have any effect on efficiency of expression in insect cells:

- Hills D, Crane-Robinson C (1995) Baculovirus expression of human basic fibroblast growth factor from a synthetic gene: role of the Kozak consensus and comparison with bacterial expression.
- Biochim Biophys Acta 1260(1):14-20.
- Ranjan A, Hasnain SE (1995) Influence of codon usage and translational initiation codon context in the AcNPV-based expression system: computer analysis using homologous and heterologous genes. Virus Genes 9(2):149-153.

Do I need to include a ribosomal binding site (RBS/Shine Dalgarno sequence) or Kozak sequence when I clone my gene of interest?

ATG is often sufficient for efficient translation initiation although it depends upon the gene of interest. The best advice is to keep the native start site found in the cDNA unless one knows that it is not functionally ideal. If concerned about expression, it is advisable to test two constructs, one with the native start site and the other with a Shine Dalgarno sequence/RBS or consensus Kozak sequence (ACCAUGG), as the case may be. In general, all expression vectors that have an N-terminal fusion will already have a RBS or initiation site for translation.

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

Can you tell me the difference between a Shine-Dalgarno sequence and a Kozak sequence?

Prokaryotic mRNAs contain a Shine-Dalgarno sequence, also known as a ribosome binding site (RBS), which is composed of the polypurine sequence AGGAGG located just 5’ of the AUG initiation codon. This sequence allows the message to bind efficiently to the ribosome due to its complementarity with the 3’-end of the 16S rRNA. Similarly, eukaryotic (and specifically mammalian) mRNA also contains sequence information important for efficient translation. However, this sequence, termed a Kozak sequence, is not a true ribosome binding site, but rather a translation initiation enhancer. The Kozak consensus sequence is ACCAUGG, where AUG is the initiation codon. A purine (A/G) in position -3 has a dominant effect; with a pyrimidine (C/T) in position -3, translation becomes more sensitive to changes in positions -1, -2, and +4. Expression levels can be reduced up to 95% when the -3 position is changed from a purine to pyrimidine. The +4 position has less influence on expression levels where approximately 50% reduction is seen. See the following references:

- Kozak, M. (1986) Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes. Cell 44, 283-292.
- Kozak, M. (1987) At least six nucleotides preceding the AUG initiator codon enhance translation in mammalian cells. J. Mol. Biol. 196, 947-950.
- Kozak, M. (1987) An analysis of 5´-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 15, 8125-8148.
- Kozak, M. (1989) The scanning model for translation: An update. J. Cell Biol. 108, 229-241.
- Kozak, M. (1990) Evaluation of the fidelity of initiation of translation in reticulocyte lysates from commercial sources. Nucleic Acids Res. 18, 2828.

Note: The optimal Kozak sequence for Drosophila differs slightly, and yeast do not follow this rule at all. See the following references:

- Romanos, M.A., Scorer, C.A., Clare, J.J. (1992) Foreign gene expression in yeast: a review. Yeast 8, 423-488.
- Cavaneer, D.R. (1987) Comparison of the consensus sequence flanking translational start sites in Drosophila and vertebrates. Nucleic Acids Res. 15, 1353-1361.

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

引用および参考文献 (1)

引用および参考文献
Abstract
Proteolysis of CCN1 by plasmin: functional implications.
Authors:Pendurthi UR,Tran TT,Post M,Rao LV
Journal:Cancer research
PubMed ID:16266990
Plasmin is shown to play a crucial role in many pathophysiological processes, primarily through its ability to degrade extracellular matrix and/or mobilizing growth factors that are sequestered in the extracellular matrix. CCN1 is a matricellular protein whose expression is upregulated in cancer and various vascular diseases. The present study was ... More