Study design | execution | one-stop sourcing
Turn the research objective into a clear experimental path, equipment-reagent-consumable list, essential controls, quality documentation and delivery plan—all on one platform from design and services to formal quotation.
Start from your need
Enter through 12 disease and translational research areas to define targets, models, samples and orthogonal validation.
Open this route 02 · By experimentUse thirty end-to-end workflows to review steps, material roles, controls, QC, troubleshooting and products.
Open this route 03 · By productUse the structured catalog to define specifications, application, quality grade and documentation for a combined inquiry.
Open this route 04 · By projectConnect to protein, antibody, gene, qPCR, cell, flow cytometry, ELISA and sourcing-integration services.
Open this routeCore executable solutions
A one-stop experimental framework covering sample lysis, protein quantification, SDS-PAGE, membrane transfer, antibody incubation, signal acquisition, and data analysis.
A complete experimental framework covering sample preservation, RNA extraction, genomic DNA removal, quality assessment, reverse transcription, real-time quantitative PCR, and data analysis.
A one-stop experimental framework covering culture system selection, cell resuscitation, inoculation, media changes, passaging, counting, cryopreservation, contamination monitoring, and quality recording.
A complete research workflow from sample fixation, permeabilization, and blocking, to antibody fluorescent staining, microscopic imaging, and quantitative analysis, suitable for single-label, multi-label, and co-localization experiments.
A complete protocol covering FFPE or frozen tissue section processing, antigen retrieval, antibody staining, counterstaining, mounting, scanning, and quantitative pathological analysis for research.
Multiparameter flow cytometry solutions ranging from Panel design, sample preparation, and surface or intracellular staining, to compensation, acquisition, gating, and statistical analysis.
Covers the complete ELISA workflow, including sample coverage and range assessment, plate layout design, standard curve, sample addition and incubation, washing and color development, plate reading, fitting, and...
A one-stop protein preparation solution from host and vector selection, small-scale screening, and culture amplification, to affinity capture, chromatography polishing, buffer exchange and concentration, and quality control.
High-quality DNA that meets the requirements for PCR, cloning, sequencing, and quantitative analysis can be obtained from cells, tissues, blood, microorganisms, or reaction systems.
Obtain high-quality RNA suitable for reverse transcription, RT-qPCR, RNA-seq, and hybridization analysis from cells, tissues, and biological samples.
From target sequence amplification, vector preparation, ligation or assembly, transformation, screening, to sequencing confirmation, obtain traceable recombinant clones.
Convert DNA or RNA samples into sequencable libraries with correct fragment distribution, adapters, indexes, and quantitative results.
Design and implement gene knockout, precise editing, or regulatory experiments to establish engineered cell models with genotypic, protein, and functional evidence.
Efficiently deliver plasmids, mRNA, siRNA, oligonucleotides, or gene-editing components into cells to achieve reproducible expression or silencing effects while controlling toxicity.
Quantitatively compare the effects of treatments on cell metabolic activity, membrane integrity, proliferation, and survival to establish reliable dose-response and time-response relationships.
Differentiate early apoptosis, late apoptosis, necrosis, and other regulated cell deaths, and establish mechanisms of action through time-series and multi-indicator evidence.
Enrich target proteins and their interaction complexes from cell or tissue lysates, and validate candidate protein interactions using Western Blot, mass spectrometry, or other orthogonal methods.
Detect the enrichment of transcription factors, histone modifications, or chromatin proteins at target genomic regions, and provide traceable samples for ChIP-qPCR or ChIP-seq.
Quantitatively assess the regulation of reporter gene expression by promoters, enhancers, transcription factors, signaling pathways, or miRNAs, and correct for transfection and cell number differences using an internal...
Quantitatively compare cell migration and matrix invasion capabilities in 2D scratch or Transwell models, and evaluate the impact of genes, pathways, or candidate compounds on motile phenotypes.
To establish three-dimensional organoid models that are expandable, cryopreservable, and possess tissue-related structural and functional characteristics from tissues, adult stem cells, or pluripotent stem cells.
Microbial DNA extraction, 16S region amplification, library construction, sequencing, and community composition analysis from fecal, environmental, tissue, or low-biomass samples.
Establish an automated, quantifiable cellular or biochemical assay system with sufficient dynamic range to perform primary screening, hit confirmation, dose-response, and counter-screening of compounds.
Prepare high-viability single-cell suspensions from tissue or cell samples, perform cell counting, microdroplet or plate-based partitioning, barcoding, library construction, and pre-sequencing quality control.
Capture region- or cell-scale transcripts while preserving tissue spatial location and morphological information, completing tissue quality assessment, section optimization, spatial capture, library construction, and pre-sequencing quality control.
Perform protein extraction, reduction and alkylation, enzymatic digestion, peptide purification, quantitative strategy selection, LC-MS/MS acquisition, and data quality assessment from cells, tissues, biological fluids, or purified samples.
Absolute quantification of DNA or RNA targets without a standard curve, for method development and quality control in copy number, low-frequency variation, residual nucleic acids, vector titer, or...
Synchronously quantify multiple cytokines, chemokines, or immune markers in limited volumes of serum, plasma, cell culture supernatants, or other samples, and generate comparable immune profiles.
We perform microbial isolation, culturing, purification, phenotypic or molecular identification, and standardized antimicrobial susceptibility testing from suitable samples, providing traceable results for research, method development, and quality studies.
Select or establish appropriate animal models based on clear scientific questions, and complete study design, randomization, drug administration, observation, sample collection, endpoint evaluation, and traceable data quality control.
A consistent solution blueprint
Defines the research objective, endpoints, intended users, application boundaries and success criteria.
Confirms species, sample type, input amount, model status, instrumentation and safety conditions.
Lists critical steps, parameters, timing, temperatures, storage requirements and stage gates.
Maps every step to required materials, recommended specifications, alternatives and estimated quantities.
Sets positive, negative, blank, reference and replicate controls with acceptance and failure-review paths.
Confirms CoA, SDS, validation data, batch traceability, packaging, logistics, lead time and quotation.
Inquiry preparation checklist
From research question to complete list
For research use only (RUO). Solutions must be confirmed for the specific samples, platforms, institutional requirements and biosafety conditions. Final specifications, feasibility, pricing and lead time are subject to formal quotation.