pDisplay™ Mammalian Expression Vector
Product Image
Invitrogen™

pDisplay™ Mammalian Expression Vector

pDisplay™は、哺乳類細胞の表面への組換えタンパク質のターゲット化のために設計された哺乳類発現ベクターです。表示されているタンパク質について、既知のリガンドまたは推定されるリガンドとのと相互作用を行うための能力を分析できます。ベクターを用いたフレーム内の目的遺伝子のクローニングベクターに固有のN末端分泌シグナルおよび血小板由来の成長因子受容体(PDGFR)のC末端膜貫通アンカードメインがあるフレーム内の目的の遺伝子をクローニングすることによって、目的のタンパク質をターゲットにして、細胞表面に固定します。原核細胞でのみ作用するファージ表示ベクターとは対照的に詳細を見る
製品番号(カタログ番号)数量
V6602020 μg
製品番号(カタログ番号) V66020
価格(JPY)
71,200
キャンペーン価格
Ends: 27-Mar-2026
101,800
割引額 30,600 (30%)
20 µg
お問い合わせください ›
数量:
20 μg
pDisplay™は、哺乳類細胞の表面への組換えタンパク質のターゲット化のために設計された哺乳類発現ベクターです。表示されているタンパク質について、既知のリガンドまたは推定されるリガンドとのと相互作用を行うための能力を分析できます。ベクターを用いたフレーム内の目的遺伝子のクローニングベクターに固有のN末端分泌シグナルおよび血小板由来の成長因子受容体(PDGFR)のC末端膜貫通アンカードメインがあるフレーム内の目的の遺伝子をクローニングすることによって、目的のタンパク質をターゲットにして、細胞表面に固定します。原核細胞でのみ作用するファージ表示ベクターとは対照的に、pDisplayベクターには哺乳類細胞で処理される目的のタンパク質を表示できるという利点があります。そのため、pDisplayから発現される真核生物由来の組換えタンパク質は、天然の形態により近くなります。これにより、より正確なリガンド結合相互作用が得られる可能性があります。pDisplay™ベクターには、N末端細胞表面のターゲット指定シグナルおよびC末端膜貫通アンカードメインに加えて、以下の主要な特長があります。

•センスRNAのin vitro転写およびインサートのシーケンシング用のT7プロモーター/プライミング部位
• Geneticin™を使用した哺乳類細胞での安定した選択のためのネオマイシン耐性マーカー
• ラージT抗原(COS-1やCOS-7など)を発現する細胞株内での複製および単純なベクターレスキュー用のSV40起源
大腸菌での選択用のアンピシリン耐性遺伝子
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
供給タイプTransfection
製品タイプ哺乳類発現用ベクター
数量20 μg
選択剤(真核生物)Geneticin™(G-418)
ベクターpDisplay
クローニング法制限酵素/MCS
製品ラインpDISPLAY
プロモーターCMV
タンパク質タグIgKリーダー配列、PdGFR膜貫通ドメイン、c-Mycエピトープタグ、HAタグ, PDGFR Transmembrane Domain, c-Myc Epitope Tag, HA Tag
Unit Size20 µg
組成および保存条件
20 μg pDisplayベクターは超らせん型であり、TEバッファー、pH 8.0で0.5 μg/mL溶液として供給されます。-20℃で保存適切に保存した場合、6カ月間安定しています。

よくあるご質問(FAQ)

I used the pDisplay vector to express my protein on the cell surface. I'm able to detect the protein on a western blot using anti-HA antibody, but not with immunofluorescence using anti-myc antibody. Can you please help troubleshoot?

We would recommend checking to make sure that the gene of interest is cloned in-frame with the Platelet-derived Growth Factor Receptor (PDGFR) transmembrane domain.

Can I use FACS cell sorting or magnetic bead-based methods to isolate my cells transfected with the pDisplay vector?

When we tried FACS cell sorting of pDisplay-transfected cells using our anti-myc antibody, the sorting was not very efficient. However, pDisplay-transfected cells can be isolated using magnetic beads by first incubating the cells with anti-myc antibody and then incubating the cell-antibody complex with magnetic beads that have anti-mouse IgG1 conjugated to them. The cell can then be isolated using a magnet.

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

I used pDisplay vector to express a cell surface receptor protein. Should I be concerned about digestion of the protein during trypsinization of the cells?

Trypsin digests proteins at arginine or lysine residues, and it is widely accepted that the extracellular domains of membrane proteins are digested upon trypsinization of cells. But typically these proteins are rapidly replaced once the trypsin is removed. As an alternative to trypsin, you can remove most adherent cells using Versene (Cat. No. 15040066), which is a sterile 0.5 mM EDTA solution in PBS, and/or scraping. The EDTA chelates any free Mg2+ or Ca2+ ions, which are necessary for maintaining many cell attachments. Cell Dissociation Buffer, Enzyme-free, Hank's-based (Cat. No. 13150016) or PBS-based (Cat. No. 13151014), which are cocktails of chelating agents, are also fine for this application and may be more effective than EDTA alone, and would be unlikely to adversely affect the receptor protein.

If I transfect empty pDisplay vector into mammalian cells, will it result in a cell membrane-targeted polypeptide?

Transfection of pDisplay vector alone into mammalian cells does not result in a displayed polypeptide because the Ig kappa signal peptide and the PDGFR transmembrane domain are not in the same reading frame, and the ORF containing the kappa signal peptide ends 5 bp before the start of what is defined as the PDGFR transmembrane domain.

I heard that you carry a vector to help secrete my protein so it is targeted to the cell membrane. Which one is it?

We offer the pDisplay vector, Cat. No. V66020, designed to target recombinant proteins to the surface of mammalian cells. It contains an N-terminal murine Ig kappa-chain secretion signal and a C-terminal transmembrane anchoring domain from Platelet-derived Growth Factor Receptor (PDGFR) to target and anchor the protein of interest to the cell surface.

引用および参考文献 (6)

引用および参考文献
Abstract
Delta/notch-like epidermal growth factor (EGF)-related receptor, a novel EGF-like repeat-containing protein targeted to dendrites of developing and adult central nervous system neurons.
Authors: Eiraku Mototsugu; Hirata Yutaka; Takeshima Hiroshi; Hirano Tomoo; Kengaku Mineko;
Journal:J Biol Chem
PubMed ID:11950833
'We have identified a novel epidermal growth factor (EGF)-like repeat-containing single-pass transmembrane protein that is specifically expressed in the developing and mature central nervous system. Sequence analysis revealed that the 10 EGF-like repeats in the extracellular domain are closely related to those of the developmentally important receptor Notch and its ... More
Molecular mechanisms of pre-T cell receptor-induced survival.
Authors:Murga C, Barber DF
Journal:J Biol Chem
PubMed ID:12114514
'En route to maturing as T cell receptor (TCR) alphabeta-expressing cells, the development of thymocytes is contingent on expression of a pre-TCR complex comprising a TCRbeta chain paired with a surrogate TCRalpha chain, pre-Talpha (pTalpha). The pre-TCR has been proposed to promote cell survival, proliferation, differentiation, and lineage commitment. However, ... More
Myelin-associated glycoprotein interacts with the Nogo66 receptor to inhibit neurite outgrowth.
Authors: Domeniconi Marco; Cao Zixuan; Spencer Timothy; Sivasankaran Rajeev; Wang Kevin; Nikulina Elena; Kimura Noriko; Cai Hong; Deng Kangwen; Gao Ying; He Zhigang; Filbin Marie;
Journal:Neuron
PubMed ID:12160746
Myelin inhibitors of axonal regeneration, like Nogo and MAG, block regrowth after injury to the adult CNS. While a GPI-linked receptor for Nogo (NgR) has been identified, MAG's receptor is unknown. We show that MAG inhibits regeneration by interaction with NgR. Binding of and inhibition by MAG are lost if ... More
DNA immunization of mice and macaques with plasmids encoding hepatitis C virus envelope E2protein expressed intracellularly and on the cell surface.
Authors:Forns X, Emerson SU, Tobin GJ, Mushahwar IK, Purcell RH, Bukh J
Journal:Vaccine
PubMed ID:10217599
We analyzed the humoral immune response elicited by hepatitis C virus (HCV) E2 protein expressed in vivo after injection of plasmid DNA into mice and rhesus macaques. Three plasmids were used for immunization: a plasmid containing the entire sequence of the E2 and p7 genes (pE2); a plasmid encoding a ... More
Distinct kinetics for binding of the CD46 and SLAM receptors to overlapping sites in the measles virus hemagglutinin protein.
Authors: Santiago Cesar; Björling Ewa; Stehle Thilo; Casasnovas José M;
Journal:J Biol Chem
PubMed ID:12065582
Measles virus (MV) is a human pathogen using two distinct cell surface receptors for entry into host cells. We present here a comparative analysis for binding of the MV receptors CD46 and SLAM to the measles virus hemagglutinin protein (MVH, Edmonston strain). Soluble monomeric and dimeric MVH variants were prepared ... More