pcdna5 frt v5 his vector  (Thermo Fisher)


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    Name:
    pcDNA 5 FRT V5 His TOPO TA Expression Kit
    Description:
    Using restriction enzymes to clone your gene into an expression vector often forces you to compromise the final sequence of your insert Figure 1A especially when there are no useful restriction sites close to your genes coding sequence This may result in suboptimal spacing of expression elements or incorporation of non native amino acid residues which can reduce your expression levels and or cause the production of non functional protein In addition to being a more effective way to clone TOPO Cloning eliminates these potential expression problems TOPO Expression Vectors enable you to insert the exact DNA sequence you require simply by performing PCR with appropriately designed primers Your PCR product is cloned at a high efficiency in only five minutes into a topoisomerase I activated expression vector The resulting recombinant expression vector contains your exact DNA sequence without any non coding regions Figure 1B Many of Invitrogen s powerful expression vectors are available adapted for one step TOPO cloning and expression of PCR products In addition several expression vectors are now adapted for Directional TOPO Cloning enabling you to use proofreading polymerases and to clone your PCR products in a specific orientation
    Catalog Number:
    K602001
    Price:
    None
    Category:
    DNA Vectors Clones Purified Nucleic Acids Libraries
    Applications:
    Constitutive Expression|Mammalian Expression|Protein Biology|Protein Expression|Targeted Integration
    Buy from Supplier


    Structured Review

    Thermo Fisher pcdna5 frt v5 his vector
    Using restriction enzymes to clone your gene into an expression vector often forces you to compromise the final sequence of your insert Figure 1A especially when there are no useful restriction sites close to your genes coding sequence This may result in suboptimal spacing of expression elements or incorporation of non native amino acid residues which can reduce your expression levels and or cause the production of non functional protein In addition to being a more effective way to clone TOPO Cloning eliminates these potential expression problems TOPO Expression Vectors enable you to insert the exact DNA sequence you require simply by performing PCR with appropriately designed primers Your PCR product is cloned at a high efficiency in only five minutes into a topoisomerase I activated expression vector The resulting recombinant expression vector contains your exact DNA sequence without any non coding regions Figure 1B Many of Invitrogen s powerful expression vectors are available adapted for one step TOPO cloning and expression of PCR products In addition several expression vectors are now adapted for Directional TOPO Cloning enabling you to use proofreading polymerases and to clone your PCR products in a specific orientation
    https://www.bioz.com/result/pcdna5 frt v5 his vector/product/Thermo Fisher
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    pcdna5 frt v5 his vector - by Bioz Stars, 2021-06
    86/100 stars

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    Related Articles

    Clone Assay:

    Article Title: Identification and Characterization of a Chitin-binding Protein Purified from Coelomic Fluid of the Lugworm Arenicola marina Defining a Novel Protein Sequence Family *
    Article Snippet: Full-length AML-1a and AML-1b cDNA including their respective signal sequences were synthesized and obtained from Genescript. .. The cDNAs were cloned into the expression vector pcDNA5/FRT/V5-His-TOPO® TA vector according to the manufacturer's recommendations (Invitrogen) and sequenced in their entirety. .. The produced pcDNA5/FRT vectors were transfected into Flp-In CHO cells (Invitrogen) using jetPEITM (Polyplus transfection).

    Article Title: Loss of fibulin-4 disrupts collagen synthesis and maturation: implications for pathology resulting from EFEMP2 mutations
    Article Snippet: .. Full-length mouse fibulin-4 including the 5′ UTR was cloned by PCR and ligated into a pcDNA5/FRT/V5-His-TOPO vector (Invitrogen). .. The fibulin4-V5 vector was co-transfected with a second vector containing Flp recombinase (pOG44, Invitrogen) into Flp-InTM -CHO cells as previously described ( ).

    Article Title: Evolutionary conservation of P-selectin glycoprotein ligand-1 primary structure and function
    Article Snippet: Forty amplification cycles were performed using the Platinum® Pfx DNA Polymerase (Invitrogen; 30 s at 94°C, 45 s at 54°C, 2 min at 72°C). .. PCR products were gel-purified, sequenced, digested with AflII/AgeI and cloned in the pcDNA5/FRT/V5-His-TOPO® expression vector containing, C-terminally, 6 × His tag (Invitrogen). α1–3 fucosyltranferase-VII (FucT-VII) mRNAs from human, bovine, pig, rat and equine neutrophils were amplified using the Superscript™ One-Step RT-PCR with platinum® Taq Kit (Invitrogen). .. Primers were derived from human and mammalian FucT-VII sequences (Table ). β-actin transcripts were used as control.

    Article Title: BAG6 regulates the quality control of a polytopic ERAD substrate
    Article Snippet: Protease inhibitor cocktail, V5–agarose, tetracycline and all other chemicals were obtained from Sigma unless stated otherwise. .. DNA plasmid construction and siRNA oligonucleotides To produce BAG–V5, BAG6 isoform 2 (UniProt ID P46379-2) was cloned into pcDNA 5.0/FRT/-V5 His-TOPO-TA vector (Invitrogen) according to the manufacturer's instructions. .. BAG6-mNLS–V5 was constructed by site-directed mutagenesis as described previously ( ).

    Article Title: ACC2 Is Expressed at High Levels Human White Adipose and Has an Isoform with a Novel N-Terminus
    Article Snippet: Cloning and expression The full-length human ACC2.v1 cDNA was amplified by PCR from human skeletal muscle Marathon-Ready cDNA (Clontech) was used as the template using the following primer pair: forward, 5′-GCCTAGGTAATGGTCTTGCTTCTTTGTCTATCTTGTCTG-3′ ; reverse, 5′-ACCGGTGGTGGAGGCCGGGCTGTCCATG-3′ . .. The amplified product was cloned into a pcDNA5/FRT/V5-His-TOPO vector (Invitrogen) with an added V5 epitope and His tags at the C-terminus, and was confirmed by sequencing. .. The plasmid was then digested with AvrII and PmeI, and the cDNA fragment was subcloned into the SpeI/EcoRV site of pEFcDNA3 (Invitrogen) vector.

    Article Title: Rapid, Nongenomic Responses to Ecdysteroids and Catecholamines Mediated by a Novel Drosophila G-Protein-Coupled Receptor
    Article Snippet: The PCR used Taq polymerase and cycling conditions of 94°C for 30 s, 55°C for 30 s, and 68°C for 2 min, for 30 cycles. .. The PCR products were ligated into either the pcDNA5/FRT/V5-His-TOPO or the pcDNA3.1/CT-GFP-TOPO vectors (Invitrogen, Paisley, UK), and several clones were obtained with the full-length sequence of the novel receptor. .. Recombinant baculoviruses were generated using Gateway Cloning Technology (Invitrogen).

    Article Title: High kallikrein-related peptidase 6 in non-small cell lung cancer cells: an indicator of tumour proliferation and poor prognosis
    Article Snippet: A549 Flp-In parental or KLK6-expressing cells were grown at 37°C in an atmosphere of 5% CO2 in RPMI-1640 Glutamax I, except Calu-1 that was cultured in McCoy’s 5a medium, containing 10% foetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin and if necessary supplemented with either 100 μg/ml zeocin or 100 μg/ml hygromycin. .. Plasmids and stable transfections The complete coding sequence of KLK6 (144–1002 bp from NM_002774) with Stop codon was amplified by PCR and integrated into the T/A cloning site of pcDNA5/FRT/V5-His TOPO (Invitrogen Corp., Cergy Pontoise, France), which contains an FRT site. .. The expression vector and the plasmid encoding the yeast Flp recombinase were co-transfected into A549 Flp-In using Lipofectamine 2000 (Invitrogen Corp.) according to the manufacturer’s instructions.

    Expressing:

    Article Title: Identification and Characterization of a Chitin-binding Protein Purified from Coelomic Fluid of the Lugworm Arenicola marina Defining a Novel Protein Sequence Family *
    Article Snippet: Full-length AML-1a and AML-1b cDNA including their respective signal sequences were synthesized and obtained from Genescript. .. The cDNAs were cloned into the expression vector pcDNA5/FRT/V5-His-TOPO® TA vector according to the manufacturer's recommendations (Invitrogen) and sequenced in their entirety. .. The produced pcDNA5/FRT vectors were transfected into Flp-In CHO cells (Invitrogen) using jetPEITM (Polyplus transfection).

    Article Title: Evolutionary conservation of P-selectin glycoprotein ligand-1 primary structure and function
    Article Snippet: Forty amplification cycles were performed using the Platinum® Pfx DNA Polymerase (Invitrogen; 30 s at 94°C, 45 s at 54°C, 2 min at 72°C). .. PCR products were gel-purified, sequenced, digested with AflII/AgeI and cloned in the pcDNA5/FRT/V5-His-TOPO® expression vector containing, C-terminally, 6 × His tag (Invitrogen). α1–3 fucosyltranferase-VII (FucT-VII) mRNAs from human, bovine, pig, rat and equine neutrophils were amplified using the Superscript™ One-Step RT-PCR with platinum® Taq Kit (Invitrogen). .. Primers were derived from human and mammalian FucT-VII sequences (Table ). β-actin transcripts were used as control.

    Plasmid Preparation:

    Article Title: Identification and Characterization of a Chitin-binding Protein Purified from Coelomic Fluid of the Lugworm Arenicola marina Defining a Novel Protein Sequence Family *
    Article Snippet: Full-length AML-1a and AML-1b cDNA including their respective signal sequences were synthesized and obtained from Genescript. .. The cDNAs were cloned into the expression vector pcDNA5/FRT/V5-His-TOPO® TA vector according to the manufacturer's recommendations (Invitrogen) and sequenced in their entirety. .. The produced pcDNA5/FRT vectors were transfected into Flp-In CHO cells (Invitrogen) using jetPEITM (Polyplus transfection).

    Article Title: Loss of fibulin-4 disrupts collagen synthesis and maturation: implications for pathology resulting from EFEMP2 mutations
    Article Snippet: .. Full-length mouse fibulin-4 including the 5′ UTR was cloned by PCR and ligated into a pcDNA5/FRT/V5-His-TOPO vector (Invitrogen). .. The fibulin4-V5 vector was co-transfected with a second vector containing Flp recombinase (pOG44, Invitrogen) into Flp-InTM -CHO cells as previously described ( ).

    Article Title: Evolutionary conservation of P-selectin glycoprotein ligand-1 primary structure and function
    Article Snippet: Forty amplification cycles were performed using the Platinum® Pfx DNA Polymerase (Invitrogen; 30 s at 94°C, 45 s at 54°C, 2 min at 72°C). .. PCR products were gel-purified, sequenced, digested with AflII/AgeI and cloned in the pcDNA5/FRT/V5-His-TOPO® expression vector containing, C-terminally, 6 × His tag (Invitrogen). α1–3 fucosyltranferase-VII (FucT-VII) mRNAs from human, bovine, pig, rat and equine neutrophils were amplified using the Superscript™ One-Step RT-PCR with platinum® Taq Kit (Invitrogen). .. Primers were derived from human and mammalian FucT-VII sequences (Table ). β-actin transcripts were used as control.

    Article Title: BAG6 regulates the quality control of a polytopic ERAD substrate
    Article Snippet: Protease inhibitor cocktail, V5–agarose, tetracycline and all other chemicals were obtained from Sigma unless stated otherwise. .. DNA plasmid construction and siRNA oligonucleotides To produce BAG–V5, BAG6 isoform 2 (UniProt ID P46379-2) was cloned into pcDNA 5.0/FRT/-V5 His-TOPO-TA vector (Invitrogen) according to the manufacturer's instructions. .. BAG6-mNLS–V5 was constructed by site-directed mutagenesis as described previously ( ).

    Article Title: ACC2 Is Expressed at High Levels Human White Adipose and Has an Isoform with a Novel N-Terminus
    Article Snippet: Cloning and expression The full-length human ACC2.v1 cDNA was amplified by PCR from human skeletal muscle Marathon-Ready cDNA (Clontech) was used as the template using the following primer pair: forward, 5′-GCCTAGGTAATGGTCTTGCTTCTTTGTCTATCTTGTCTG-3′ ; reverse, 5′-ACCGGTGGTGGAGGCCGGGCTGTCCATG-3′ . .. The amplified product was cloned into a pcDNA5/FRT/V5-His-TOPO vector (Invitrogen) with an added V5 epitope and His tags at the C-terminus, and was confirmed by sequencing. .. The plasmid was then digested with AvrII and PmeI, and the cDNA fragment was subcloned into the SpeI/EcoRV site of pEFcDNA3 (Invitrogen) vector.

    Polymerase Chain Reaction:

    Article Title: Loss of fibulin-4 disrupts collagen synthesis and maturation: implications for pathology resulting from EFEMP2 mutations
    Article Snippet: .. Full-length mouse fibulin-4 including the 5′ UTR was cloned by PCR and ligated into a pcDNA5/FRT/V5-His-TOPO vector (Invitrogen). .. The fibulin4-V5 vector was co-transfected with a second vector containing Flp recombinase (pOG44, Invitrogen) into Flp-InTM -CHO cells as previously described ( ).

    Article Title: Evolutionary conservation of P-selectin glycoprotein ligand-1 primary structure and function
    Article Snippet: Forty amplification cycles were performed using the Platinum® Pfx DNA Polymerase (Invitrogen; 30 s at 94°C, 45 s at 54°C, 2 min at 72°C). .. PCR products were gel-purified, sequenced, digested with AflII/AgeI and cloned in the pcDNA5/FRT/V5-His-TOPO® expression vector containing, C-terminally, 6 × His tag (Invitrogen). α1–3 fucosyltranferase-VII (FucT-VII) mRNAs from human, bovine, pig, rat and equine neutrophils were amplified using the Superscript™ One-Step RT-PCR with platinum® Taq Kit (Invitrogen). .. Primers were derived from human and mammalian FucT-VII sequences (Table ). β-actin transcripts were used as control.

    Article Title: Rapid, Nongenomic Responses to Ecdysteroids and Catecholamines Mediated by a Novel Drosophila G-Protein-Coupled Receptor
    Article Snippet: The PCR used Taq polymerase and cycling conditions of 94°C for 30 s, 55°C for 30 s, and 68°C for 2 min, for 30 cycles. .. The PCR products were ligated into either the pcDNA5/FRT/V5-His-TOPO or the pcDNA3.1/CT-GFP-TOPO vectors (Invitrogen, Paisley, UK), and several clones were obtained with the full-length sequence of the novel receptor. .. Recombinant baculoviruses were generated using Gateway Cloning Technology (Invitrogen).

    Article Title: High kallikrein-related peptidase 6 in non-small cell lung cancer cells: an indicator of tumour proliferation and poor prognosis
    Article Snippet: A549 Flp-In parental or KLK6-expressing cells were grown at 37°C in an atmosphere of 5% CO2 in RPMI-1640 Glutamax I, except Calu-1 that was cultured in McCoy’s 5a medium, containing 10% foetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin and if necessary supplemented with either 100 μg/ml zeocin or 100 μg/ml hygromycin. .. Plasmids and stable transfections The complete coding sequence of KLK6 (144–1002 bp from NM_002774) with Stop codon was amplified by PCR and integrated into the T/A cloning site of pcDNA5/FRT/V5-His TOPO (Invitrogen Corp., Cergy Pontoise, France), which contains an FRT site. .. The expression vector and the plasmid encoding the yeast Flp recombinase were co-transfected into A549 Flp-In using Lipofectamine 2000 (Invitrogen Corp.) according to the manufacturer’s instructions.

    Construct:

    Article Title: Engineering of CHO cells for the production of vertebrate recombinant sialyltransferases
    Article Snippet: For comparative purposes we have also constructed full-length human and zebrafish ST6Gal I expression vectors. .. These constructs, based on pcDNA5/FRT/V5-His-TOPO (Invitrogen, Carlsbad, CA, USA), do not support active secretion from CHO cells, however, the catalytic domain of ST6Gal I is detected in cell culture supernatants ( ; ). ..

    Cell Culture:

    Article Title: Engineering of CHO cells for the production of vertebrate recombinant sialyltransferases
    Article Snippet: For comparative purposes we have also constructed full-length human and zebrafish ST6Gal I expression vectors. .. These constructs, based on pcDNA5/FRT/V5-His-TOPO (Invitrogen, Carlsbad, CA, USA), do not support active secretion from CHO cells, however, the catalytic domain of ST6Gal I is detected in cell culture supernatants ( ; ). ..

    Amplification:

    Article Title: Evolutionary conservation of P-selectin glycoprotein ligand-1 primary structure and function
    Article Snippet: Forty amplification cycles were performed using the Platinum® Pfx DNA Polymerase (Invitrogen; 30 s at 94°C, 45 s at 54°C, 2 min at 72°C). .. PCR products were gel-purified, sequenced, digested with AflII/AgeI and cloned in the pcDNA5/FRT/V5-His-TOPO® expression vector containing, C-terminally, 6 × His tag (Invitrogen). α1–3 fucosyltranferase-VII (FucT-VII) mRNAs from human, bovine, pig, rat and equine neutrophils were amplified using the Superscript™ One-Step RT-PCR with platinum® Taq Kit (Invitrogen). .. Primers were derived from human and mammalian FucT-VII sequences (Table ). β-actin transcripts were used as control.

    Article Title: ACC2 Is Expressed at High Levels Human White Adipose and Has an Isoform with a Novel N-Terminus
    Article Snippet: Cloning and expression The full-length human ACC2.v1 cDNA was amplified by PCR from human skeletal muscle Marathon-Ready cDNA (Clontech) was used as the template using the following primer pair: forward, 5′-GCCTAGGTAATGGTCTTGCTTCTTTGTCTATCTTGTCTG-3′ ; reverse, 5′-ACCGGTGGTGGAGGCCGGGCTGTCCATG-3′ . .. The amplified product was cloned into a pcDNA5/FRT/V5-His-TOPO vector (Invitrogen) with an added V5 epitope and His tags at the C-terminus, and was confirmed by sequencing. .. The plasmid was then digested with AvrII and PmeI, and the cDNA fragment was subcloned into the SpeI/EcoRV site of pEFcDNA3 (Invitrogen) vector.

    Article Title: High kallikrein-related peptidase 6 in non-small cell lung cancer cells: an indicator of tumour proliferation and poor prognosis
    Article Snippet: A549 Flp-In parental or KLK6-expressing cells were grown at 37°C in an atmosphere of 5% CO2 in RPMI-1640 Glutamax I, except Calu-1 that was cultured in McCoy’s 5a medium, containing 10% foetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin and if necessary supplemented with either 100 μg/ml zeocin or 100 μg/ml hygromycin. .. Plasmids and stable transfections The complete coding sequence of KLK6 (144–1002 bp from NM_002774) with Stop codon was amplified by PCR and integrated into the T/A cloning site of pcDNA5/FRT/V5-His TOPO (Invitrogen Corp., Cergy Pontoise, France), which contains an FRT site. .. The expression vector and the plasmid encoding the yeast Flp recombinase were co-transfected into A549 Flp-In using Lipofectamine 2000 (Invitrogen Corp.) according to the manufacturer’s instructions.

    Reverse Transcription Polymerase Chain Reaction:

    Article Title: Evolutionary conservation of P-selectin glycoprotein ligand-1 primary structure and function
    Article Snippet: Forty amplification cycles were performed using the Platinum® Pfx DNA Polymerase (Invitrogen; 30 s at 94°C, 45 s at 54°C, 2 min at 72°C). .. PCR products were gel-purified, sequenced, digested with AflII/AgeI and cloned in the pcDNA5/FRT/V5-His-TOPO® expression vector containing, C-terminally, 6 × His tag (Invitrogen). α1–3 fucosyltranferase-VII (FucT-VII) mRNAs from human, bovine, pig, rat and equine neutrophils were amplified using the Superscript™ One-Step RT-PCR with platinum® Taq Kit (Invitrogen). .. Primers were derived from human and mammalian FucT-VII sequences (Table ). β-actin transcripts were used as control.

    Sequencing:

    Article Title: ACC2 Is Expressed at High Levels Human White Adipose and Has an Isoform with a Novel N-Terminus
    Article Snippet: Cloning and expression The full-length human ACC2.v1 cDNA was amplified by PCR from human skeletal muscle Marathon-Ready cDNA (Clontech) was used as the template using the following primer pair: forward, 5′-GCCTAGGTAATGGTCTTGCTTCTTTGTCTATCTTGTCTG-3′ ; reverse, 5′-ACCGGTGGTGGAGGCCGGGCTGTCCATG-3′ . .. The amplified product was cloned into a pcDNA5/FRT/V5-His-TOPO vector (Invitrogen) with an added V5 epitope and His tags at the C-terminus, and was confirmed by sequencing. .. The plasmid was then digested with AvrII and PmeI, and the cDNA fragment was subcloned into the SpeI/EcoRV site of pEFcDNA3 (Invitrogen) vector.

    Article Title: Rapid, Nongenomic Responses to Ecdysteroids and Catecholamines Mediated by a Novel Drosophila G-Protein-Coupled Receptor
    Article Snippet: The PCR used Taq polymerase and cycling conditions of 94°C for 30 s, 55°C for 30 s, and 68°C for 2 min, for 30 cycles. .. The PCR products were ligated into either the pcDNA5/FRT/V5-His-TOPO or the pcDNA3.1/CT-GFP-TOPO vectors (Invitrogen, Paisley, UK), and several clones were obtained with the full-length sequence of the novel receptor. .. Recombinant baculoviruses were generated using Gateway Cloning Technology (Invitrogen).

    Article Title: High kallikrein-related peptidase 6 in non-small cell lung cancer cells: an indicator of tumour proliferation and poor prognosis
    Article Snippet: A549 Flp-In parental or KLK6-expressing cells were grown at 37°C in an atmosphere of 5% CO2 in RPMI-1640 Glutamax I, except Calu-1 that was cultured in McCoy’s 5a medium, containing 10% foetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin and if necessary supplemented with either 100 μg/ml zeocin or 100 μg/ml hygromycin. .. Plasmids and stable transfections The complete coding sequence of KLK6 (144–1002 bp from NM_002774) with Stop codon was amplified by PCR and integrated into the T/A cloning site of pcDNA5/FRT/V5-His TOPO (Invitrogen Corp., Cergy Pontoise, France), which contains an FRT site. .. The expression vector and the plasmid encoding the yeast Flp recombinase were co-transfected into A549 Flp-In using Lipofectamine 2000 (Invitrogen Corp.) according to the manufacturer’s instructions.

    Transfection:

    Article Title: High kallikrein-related peptidase 6 in non-small cell lung cancer cells: an indicator of tumour proliferation and poor prognosis
    Article Snippet: A549 Flp-In parental or KLK6-expressing cells were grown at 37°C in an atmosphere of 5% CO2 in RPMI-1640 Glutamax I, except Calu-1 that was cultured in McCoy’s 5a medium, containing 10% foetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin and if necessary supplemented with either 100 μg/ml zeocin or 100 μg/ml hygromycin. .. Plasmids and stable transfections The complete coding sequence of KLK6 (144–1002 bp from NM_002774) with Stop codon was amplified by PCR and integrated into the T/A cloning site of pcDNA5/FRT/V5-His TOPO (Invitrogen Corp., Cergy Pontoise, France), which contains an FRT site. .. The expression vector and the plasmid encoding the yeast Flp recombinase were co-transfected into A549 Flp-In using Lipofectamine 2000 (Invitrogen Corp.) according to the manufacturer’s instructions.

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  • 93
    Thermo Fisher pcdna5 frt v5 his topo vector
    Pcdna5 Frt V5 His Topo Vector, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pcdna5 frt v5 his topo vector/product/Thermo Fisher
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    pcdna5 frt v5 his topo vector - by Bioz Stars, 2021-06
    93/100 stars
      Buy from Supplier

    99
    Thermo Fisher mammalian expression vector pcdna5 frt v5 his topo
    Mammalian Expression Vector Pcdna5 Frt V5 His Topo, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mammalian expression vector pcdna5 frt v5 his topo/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mammalian expression vector pcdna5 frt v5 his topo - by Bioz Stars, 2021-06
    99/100 stars
      Buy from Supplier

    86
    Thermo Fisher pcdna5 frt v5 his topo ta vector
    Pcdna5 Frt V5 His Topo Ta Vector, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pcdna5 frt v5 his topo ta vector/product/Thermo Fisher
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    pcdna5 frt v5 his topo ta vector - by Bioz Stars, 2021-06
    86/100 stars
      Buy from Supplier

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