№ files_lp_4_process_3_072209
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Supplementary table listing the oligonucleotide primers used for PCR amplification of genes related to Shigella isolates from pediatric patients, including gel electrophoresis results for the presence of specific genes.
Gene target:
ipaH, ipaB, ipaC, ipaD, ipgD, Sen (ShET-2), virA
Year:
Not specified
Region / City:
Not specified
Topic:
Molecular Biology / Genetics
Document Type:
Supplementary Information
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Researchers in microbiology or genetics
Date of Approval:
Not specified
Date of Modifications:
Not specified
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2023
Region / City:
China
Subject:
Molecular detection of tick-borne pathogens
Document type:
Research Supplementary Table
Author:
Liu et al., 2012; Guo et al., 2019; Hazihan et al., 2019; Li et al., 2016; Cao et al., 2013; Peng et al., 2019; Reye et al., 2012
Target audience:
Researchers, Molecular biologists
Action period:
N/A
Approval date:
N/A
Amendment date:
N/A
Note:
Year
Topic:
Genotyping and vector construction
Document Type:
Supplementary table
Target Audience:
Researchers in molecular biology
Year:
2002
Region / city:
Canada
Theme:
Molecular biology
Document type:
Scientific research data
Organization / institution:
Jones et al.
Author:
Jones et al.
Target audience:
Researchers in molecular biology
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Note:
Year
Topic:
Genetic research
Document type:
Research data
Target audience:
Researchers, scientists
Note:
Year
Theme:
Gene expression
Document Type:
Research data table
Target Audience:
Researchers in immunology
Title:
Supplementary Table 1. Primers used in this study
Subject:
Primer sequences for gene amplification
Genes analyzed:
Cyclin D1; c-myc; Wnt1; Wnt2; Wnt3a; Wnt6; Wnt7b; Wnt8a; Wnt9a; Wnt9b; Wnt10b; Frizzled 3; Frizzled 5; Frizzled 6; iNos; TNF-α; MCP-1; Arg1; Mrc-2; CD163; β-actin
Primer orientation:
Forward (F) and Reverse (R)
Type of document:
Supplementary scientific table
Field of research:
Molecular biology; Gene expression analysis
Methodological context:
Polymerase chain reaction (PCR)
Content elements:
Nucleotide sequences of forward and reverse primers
Role in publication:
Supplementary material
Year:
Not specified
Region / city:
Not specified
Theme:
Molecular biology, microbiology, genetics
Document type:
Research article
Organization / institution:
Not specified
Author:
Not specified
Target audience:
Researchers, microbiologists
Period of validity:
Not applicable
Approval date:
Not specified
Modification date:
Not specified
Document type:
Supplementary material
Content type:
List of primers and nucleotide sequences
Subject:
Gene cloning and qRT-PCR primer sequences
Techniques:
Gene cloning; qRT-PCR
Genes mentioned:
MnSOD; PotD; GPD; PA; YGIW; QseB; GA; Omp26; PT; VA; Tex; HutZ; apbE; kefA; CRP; Clpp; QueA; IL-6; TNF-α; IL-1β; GAPDH; IFN-γ; IL-2; IL-4
Sequence orientation:
5’-3’
Field of research:
Molecular biology; Gene expression analysis
Associated study:
Experimental research study (unspecified)
Year:
2026
Region / city:
Not specified
Theme:
Genetics, Molecular Biology
Document Type:
Research Supplementary Table
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Researchers in Molecular Biology
Period of Action:
Not applicable
Approval Date:
Not specified
Date of Changes:
Not specified
Context:
A supplementary table listing primers and sequences used for qRT-PCR, along with associated experimental data on gene knockdown and antibody information.
Gene:
Gene
Year:
Not specified
Region / City:
Not specified
Topic:
Primer sequences for vector construction and qRT-PCR
Document Type:
Scientific supplementary data
Institution:
Not specified
Author:
Not specified
Target Audience:
Researchers in molecular biology
Period of Effect:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Context:
Document provides detailed sequences for vector construction primers and qRT-PCR primers used in gene expression studies.
Year:
N/A
Region / city:
N/A
Theme:
Gene cloning, CRISPR, Primer design
Document type:
Supplementary file
Organization / institution:
N/A
Author:
N/A
Target audience:
Researchers in molecular biology
Validity period:
N/A
Approval date:
N/A
Modification date:
N/A
Context:
A supplementary document listing sequences of primers for gene cloning and construction of various reporter vectors related to CRISPR-based studies.
Document type:
Supplementary scientific tables
Scientific field:
Plant molecular biology
Research topic:
Gene primers and anthocyanin composition analysis
Analyzed organism:
Arabidopsis (wild-type)
Experimental methods:
qRT-PCR primer design; HPLC-DAD; HPLC-ESI-MS
Chemical compounds analyzed:
Cyanidin derivatives; Pelargonidin derivatives
Extraction solvent:
Acidic MeOH-H₂O
Analytical parameters:
Retention time, λmax values, ESI-MS m/z signals
Referenced studies:
Takayuki Tohge and Yasutaka Nishiyama et al. (2005); Stephen J. Bloor and Sharon Abrahams (2002); Wei Sun and Xiangyu Meng et al. (2016)
Year:
2026
Type of document:
Scientific supplementary material
Field:
Molecular biology / Gene expression
Target organisms:
Plant genes (specific targets: ACS, ARG7, ERF1, SGR5, RPT3, RPD1, HISTONE H3, ACTIN)
Methods:
qRT-PCR assay
Primer type:
Gene-specific primers
Amplicon size:
62–193 bp
Unigene IDs:
Unigene20575_All, Unigene20551_All, Unigene13079_All, Unigene12164_All, Unigene15061_All, Unigene20360_All, AF304365.1, GQ339772.1
Intended use:
Research replication and reference
Year:
N/A
Region/City:
N/A
Topic:
miRNA expression and sequencing primers
Document Type:
Scientific Table
Author:
N/A
Target Audience:
Researchers in genetics and molecular biology
Period of Action:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2023
Region / City:
China
Subject:
Molecular detection of tick-borne pathogens
Document type:
Research Supplementary Table
Author:
Liu et al., 2012; Guo et al., 2019; Hazihan et al., 2019; Li et al., 2016; Cao et al., 2013; Peng et al., 2019; Reye et al., 2012
Target audience:
Researchers, Molecular biologists
Action period:
N/A
Approval date:
N/A
Amendment date:
N/A
Year:
2026
Field:
Molecular biology / Gene expression analysis
Document type:
Research supplementary table
Organ / Institution:
Not specified
Target audience:
Researchers in molecular biology and genetics
Genes analyzed:
Actb, Akt2, Arnt, Atoh1, Ccnd1, Ccnd2, Cdk20, Cxcr4, Eras, Gdi2, Gli1, Gli2, Lhx1, Mycn, Pdgfb, Pdgfrb, Ptch1, Ptch2, Sfrp1
Methods:
RT-qPCR
Sequence type:
Primers and probes
Data format:
Nucleotide sequences
Year:
Not provided
Region / City:
Not specified
Topic:
Research ethics, manuscript submission
Document type:
Template
Author:
Not specified
Target audience:
Authors submitting research articles
Period of validity:
Not provided
Approval date:
Not specified
Date of changes:
Not specified
Year:
2026
Region / City:
Global
Topic:
Transboundary river research, Natural Language Processing, Named Entity Recognition, Python
Document type:
Research methodology
Organization / Institution:
None mentioned
Author:
Sahana et al.
Target audience:
Researchers in the field of natural language processing and transboundary river studies
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Year:
2023
Region / City:
N/A
Topic:
Education, Learning Disabilities
Document Type:
Report
Organization:
N/A
Author:
N/A
Target Audience:
Educators, Special Education Teachers
Period of Action:
N/A
Approval Date:
N/A
Modification Date:
N/A