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plasmid ppiczαa  (ATCC)


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    Structured Review

    ATCC plasmid ppiczαa
    Figure 1. Construction of the PBD2 expression plasmid and its P. pastoris transformants. (A) Codon- optimized cDNA sequence of PBD2 for P. pastoris (upper line) and its corresponding amino acid sequence (lower line). *, stop codon. (B) Schematic diagram of recombinant plasmid pPPBD2. (C) PCR identification of pPPBD2. M, Marker; 1–2, plasmid <t>pPICZαA;</t> 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213. M, Marker; 1–2, positive transformants; 3–4, P. pastoris X33; 5–6, pPPBD2 plasmid; 7, negative control.
    Plasmid Ppiczαa, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 19844 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/plasmid ppiczαa/product/ATCC
    Average 99 stars, based on 19844 article reviews
    plasmid ppiczαa - by Bioz Stars, 2026-06
    99/100 stars

    Images

    1) Product Images from "Porcine β-Defensin 2 Expressed in Pichia pastoris Alleviates Enterotoxigenic Escherichia coli -Induced Intestinal Injury and Inflammatory Response in Mice."

    Article Title: Porcine β-Defensin 2 Expressed in Pichia pastoris Alleviates Enterotoxigenic Escherichia coli -Induced Intestinal Injury and Inflammatory Response in Mice.

    Journal: Animals : an open access journal from MDPI

    doi: 10.3390/ani15101389

    Figure 1. Construction of the PBD2 expression plasmid and its P. pastoris transformants. (A) Codon- optimized cDNA sequence of PBD2 for P. pastoris (upper line) and its corresponding amino acid sequence (lower line). *, stop codon. (B) Schematic diagram of recombinant plasmid pPPBD2. (C) PCR identification of pPPBD2. M, Marker; 1–2, plasmid pPICZαA; 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213. M, Marker; 1–2, positive transformants; 3–4, P. pastoris X33; 5–6, pPPBD2 plasmid; 7, negative control.
    Figure Legend Snippet: Figure 1. Construction of the PBD2 expression plasmid and its P. pastoris transformants. (A) Codon- optimized cDNA sequence of PBD2 for P. pastoris (upper line) and its corresponding amino acid sequence (lower line). *, stop codon. (B) Schematic diagram of recombinant plasmid pPPBD2. (C) PCR identification of pPPBD2. M, Marker; 1–2, plasmid pPICZαA; 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213. M, Marker; 1–2, positive transformants; 3–4, P. pastoris X33; 5–6, pPPBD2 plasmid; 7, negative control.

    Techniques Used: Expressing, Plasmid Preparation, Sequencing, Recombinant, Marker, Negative Control, Inhibition

    Figure 2. Expression of PBD2 in P. pastoris. (A) Preliminary screening of positive transformants. In total, 100 µL supernatant of different transformants was co-incubated with 100 µL S. aureus ATCC 29213 with an OD600 of 0.02, and the OD600 was measured after 8 h. Inhibition ratios greater than 15% are shown. (B) Secondary screening of positive transformants. In total, 500 µL supernatant was co-incubated with 500 µL ATCC 29213 (5 × 105 CFU/mL) for 1 h at 37 ◦C without shaking, and 100 µL from each sample was withdrawn to count the bacterial number. (C) Tricine SDS- PAGE analysis of rPBD2-51 with 1% methanol induction for 72 h. M, Marker; 1, 15 µL supernatant from the transformant which harbors the pPICZαA vector; 2, 15 µL supernatant from rPBD2-51. (D) Western blot analysis of rPBD2-51 using PBD2 monoclonal antibody. M, Marker; 1, pPICZαA vector supernatant; 2, rPBD2-51 supernatant. (E) The rPBD2 supernatant inhibits the growth of ATCC 29213. 1, The supernatant from the transformant which harbors the pPICZαA vector; 2, The supernatant from rPBD2-51; 3, Ampicillin.
    Figure Legend Snippet: Figure 2. Expression of PBD2 in P. pastoris. (A) Preliminary screening of positive transformants. In total, 100 µL supernatant of different transformants was co-incubated with 100 µL S. aureus ATCC 29213 with an OD600 of 0.02, and the OD600 was measured after 8 h. Inhibition ratios greater than 15% are shown. (B) Secondary screening of positive transformants. In total, 500 µL supernatant was co-incubated with 500 µL ATCC 29213 (5 × 105 CFU/mL) for 1 h at 37 ◦C without shaking, and 100 µL from each sample was withdrawn to count the bacterial number. (C) Tricine SDS- PAGE analysis of rPBD2-51 with 1% methanol induction for 72 h. M, Marker; 1, 15 µL supernatant from the transformant which harbors the pPICZαA vector; 2, 15 µL supernatant from rPBD2-51. (D) Western blot analysis of rPBD2-51 using PBD2 monoclonal antibody. M, Marker; 1, pPICZαA vector supernatant; 2, rPBD2-51 supernatant. (E) The rPBD2 supernatant inhibits the growth of ATCC 29213. 1, The supernatant from the transformant which harbors the pPICZαA vector; 2, The supernatant from rPBD2-51; 3, Ampicillin.

    Techniques Used: Expressing, Incubation, Inhibition, SDS Page, Marker, Plasmid Preparation, Western Blot



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    Figure 1. Construction of the PBD2 expression plasmid and its P. pastoris transformants. (A) Codon- optimized cDNA sequence of PBD2 for P. pastoris (upper line) and its corresponding amino acid sequence (lower line). *, stop codon. (B) Schematic diagram of recombinant plasmid pPPBD2. (C) PCR identification of pPPBD2. M, Marker; 1–2, plasmid <t>pPICZαA;</t> 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213. M, Marker; 1–2, positive transformants; 3–4, P. pastoris X33; 5–6, pPPBD2 plasmid; 7, negative control.
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    Image Search Results


    Figure 1. Construction of the PBD2 expression plasmid and its P. pastoris transformants. (A) Codon- optimized cDNA sequence of PBD2 for P. pastoris (upper line) and its corresponding amino acid sequence (lower line). *, stop codon. (B) Schematic diagram of recombinant plasmid pPPBD2. (C) PCR identification of pPPBD2. M, Marker; 1–2, plasmid pPICZαA; 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213. M, Marker; 1–2, positive transformants; 3–4, P. pastoris X33; 5–6, pPPBD2 plasmid; 7, negative control.

    Journal: Animals : an open access journal from MDPI

    Article Title: Porcine β-Defensin 2 Expressed in Pichia pastoris Alleviates Enterotoxigenic Escherichia coli -Induced Intestinal Injury and Inflammatory Response in Mice.

    doi: 10.3390/ani15101389

    Figure Lengend Snippet: Figure 1. Construction of the PBD2 expression plasmid and its P. pastoris transformants. (A) Codon- optimized cDNA sequence of PBD2 for P. pastoris (upper line) and its corresponding amino acid sequence (lower line). *, stop codon. (B) Schematic diagram of recombinant plasmid pPPBD2. (C) PCR identification of pPPBD2. M, Marker; 1–2, plasmid pPICZαA; 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213. M, Marker; 1–2, positive transformants; 3–4, P. pastoris X33; 5–6, pPPBD2 plasmid; 7, negative control.

    Article Snippet: M, Marker; 1–2, plasmid pPICZαA; 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213.

    Techniques: Expressing, Plasmid Preparation, Sequencing, Recombinant, Marker, Negative Control, Inhibition

    Figure 2. Expression of PBD2 in P. pastoris. (A) Preliminary screening of positive transformants. In total, 100 µL supernatant of different transformants was co-incubated with 100 µL S. aureus ATCC 29213 with an OD600 of 0.02, and the OD600 was measured after 8 h. Inhibition ratios greater than 15% are shown. (B) Secondary screening of positive transformants. In total, 500 µL supernatant was co-incubated with 500 µL ATCC 29213 (5 × 105 CFU/mL) for 1 h at 37 ◦C without shaking, and 100 µL from each sample was withdrawn to count the bacterial number. (C) Tricine SDS- PAGE analysis of rPBD2-51 with 1% methanol induction for 72 h. M, Marker; 1, 15 µL supernatant from the transformant which harbors the pPICZαA vector; 2, 15 µL supernatant from rPBD2-51. (D) Western blot analysis of rPBD2-51 using PBD2 monoclonal antibody. M, Marker; 1, pPICZαA vector supernatant; 2, rPBD2-51 supernatant. (E) The rPBD2 supernatant inhibits the growth of ATCC 29213. 1, The supernatant from the transformant which harbors the pPICZαA vector; 2, The supernatant from rPBD2-51; 3, Ampicillin.

    Journal: Animals : an open access journal from MDPI

    Article Title: Porcine β-Defensin 2 Expressed in Pichia pastoris Alleviates Enterotoxigenic Escherichia coli -Induced Intestinal Injury and Inflammatory Response in Mice.

    doi: 10.3390/ani15101389

    Figure Lengend Snippet: Figure 2. Expression of PBD2 in P. pastoris. (A) Preliminary screening of positive transformants. In total, 100 µL supernatant of different transformants was co-incubated with 100 µL S. aureus ATCC 29213 with an OD600 of 0.02, and the OD600 was measured after 8 h. Inhibition ratios greater than 15% are shown. (B) Secondary screening of positive transformants. In total, 500 µL supernatant was co-incubated with 500 µL ATCC 29213 (5 × 105 CFU/mL) for 1 h at 37 ◦C without shaking, and 100 µL from each sample was withdrawn to count the bacterial number. (C) Tricine SDS- PAGE analysis of rPBD2-51 with 1% methanol induction for 72 h. M, Marker; 1, 15 µL supernatant from the transformant which harbors the pPICZαA vector; 2, 15 µL supernatant from rPBD2-51. (D) Western blot analysis of rPBD2-51 using PBD2 monoclonal antibody. M, Marker; 1, pPICZαA vector supernatant; 2, rPBD2-51 supernatant. (E) The rPBD2 supernatant inhibits the growth of ATCC 29213. 1, The supernatant from the transformant which harbors the pPICZαA vector; 2, The supernatant from rPBD2-51; 3, Ampicillin.

    Article Snippet: M, Marker; 1–2, plasmid pPICZαA; 3–4, pPPBD2; 5, negative control. (D) Identification of P. pastoris transformants that have the highest inhibition rate against ATCC 29213.

    Techniques: Expressing, Incubation, Inhibition, SDS Page, Marker, Plasmid Preparation, Western Blot

    Summary of the purification of  recombinant  Arthrobacter sp. S3* Bgal2 and Bgal42 β- d -galactosidases obtained from 1 L of E. coli LMG194 culture.

    Journal: International Journal of Molecular Sciences

    Article Title: Heterologous Production, Purification and Characterization of Two Cold-Active β- d -Galactosidases with Transglycosylation Activity from the Psychrotolerant Arctic Bacterium Arthrobacter sp. S3* Isolated from Spitsbergen Island Soil

    doi: 10.3390/ijms252413354

    Figure Lengend Snippet: Summary of the purification of recombinant Arthrobacter sp. S3* Bgal2 and Bgal42 β- d -galactosidases obtained from 1 L of E. coli LMG194 culture.

    Article Snippet: The resulting pPICZαA/GH42βGalS3*I recombinant plasmid was linearized with Mss I ( Pme I) enzyme and transformed into K. phaffii X-33 cells (Invitrogen, Carlsbad, CA, USA) by electroporation.

    Techniques: Purification, Recombinant, Activity Assay