№ files_lp_4_process_2_89842
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This document lists oligonucleotide primers used for molecular detection of various tick-borne pathogens in different regions of China.
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
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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
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:
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:
2026
Region / city:
N/A
Subject:
Molecular biology
Document type:
Research data
Organization:
N/A
Author:
N/A
Target audience:
Researchers in molecular biology
Period of validity:
N/A
Approval date:
N/A
Modification date:
N/A
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