Biocytogen
CRO · In Vitro Pharmacology, Target ID & Validation, Biomarker Discovery & Development
Protein Sciences and Reagents covers making the proteins and antibodies a discovery program runs on: gene-to-protein expression, purification, and custom reagent supply. You need it early in discovery, before assays, screening, and structural work can start. On BioBridgeX, buyers source and compare qualified CROs under one contract, free for buyers.
CRO · In Vitro Pharmacology, Target ID & Validation, Biomarker Discovery & Development
CRO · Target ID & Validation, Assay Development & Screening, Hit-to-Lead
CRO & CDMO · Assay Development & Screening, Hit-to-Lead, Lead Optimization
CRO · Assay Development & Screening, Hit-to-Lead, Lead Optimization
CRO & CDMO · Assay Development & Screening, Protein Sciences & Reagents, Medicinal & Synthetic Chemistry
CRO · Assay Development & Screening, Hit-to-Lead, Structural Biology
CRO · Assay Development & Screening, Hit-to-Lead, Lead Optimization
CRO · Assay Development & Screening, Hit-to-Lead, Lead Optimization
CRO & CDMO · Target ID & Validation, Assay Development & Screening, Hit-to-Lead
CRO · Target ID & Validation, Assay Development & Screening, Hit-to-Lead
CRO · Target ID & Validation, Assay Development & Screening, Hit-to-Lead
CRO · Target ID & Validation, Assay Development & Screening, Hit-to-Lead
CRO & CDMO · DMPK / ADME, GLP Toxicology, Safety Pharmacology
CRO & CDMO · In Vitro / Early Toxicology, DMPK / ADME, Safety Pharmacology
CRO · Assay Development & Screening, In Vitro Pharmacology, Target ID & Validation
CRO · In Vitro / Early Toxicology, Safety Pharmacology, DMPK / ADME
CRO & CDMO · GLP Toxicology, Safety Pharmacology, Genetic Toxicology
CRO & CDMO · GLP Toxicology, Safety Pharmacology, Genetic Toxicology
Protein Sciences and Reagents is the supply line that feeds the rest of discovery. Before you can run a binding assay, screen a library, solve a structure, or characterize a candidate, you need the actual protein in a tube: your target expressed and purified, the right reference reagents, and often a custom antibody or two. A CRO in this category designs the construct, picks an expression system, makes the protein, purifies it to the quality your downstream work demands, and ships you material you can trust. It sounds like plumbing, and in a sense it is, but a badly behaved protein quietly poisons every experiment that touches it.
You reach for this work at the very front of a program, usually in parallel with assay development rather than after it. The typical triggers are concrete: you have a new target and need milligram quantities of active, correctly folded protein for an assay; you need a panel of mutants or a tagged construct for an SPR or crystallography campaign; you need a custom polyclonal or monoclonal antibody as a detection reagent; or you need a hard-to-express membrane protein or multi-domain complex that your own lab has tried and failed to make. Many small biotechs simply do not own the fermentation, chromatography, and antibody-generation capacity to do this at the scale and quality a real screening or structural effort needs, so they outsource it.
The work spans expression systems and protein classes. E. coli for straightforward soluble proteins, baculovirus or insect cells and mammalian (HEK or CHO) systems for proteins that need glycosylation or proper folding, and cell-free systems for tricky cases. On the protein side this covers enzymes, kinases, receptors, antibodies and antibody fragments, fusion proteins, and the membrane proteins that are notoriously stubborn to express. On the reagent side it covers custom antibody generation (polyclonal, monoclonal, and increasingly recombinant), antibody conjugation and labeling, and reference standards. Most of this is research-grade work conducted under good documentation rather than GLP or GMP, though material destined for a regulated assay carries tighter quality expectations.
The core deliverable is purified protein, and the path to it is more involved than "express and purify." A capable vendor takes a sequence or a target idea and works backward through construct design (tags, truncations, codon optimization, signal sequences), chooses and optimizes an expression system, scales the culture, then runs a purification train (affinity, ion exchange, size exclusion) to hit your purity and endotoxin targets. Just as important is the characterization that proves the protein is real: SDS-PAGE and Western blot for identity and purity, mass spec for intact mass, SEC-MALS or analytical ultracentrifugation for aggregation state and oligomerization, and a functional or activity assay to confirm the protein actually works, not just that it exists. A protein that runs clean on a gel but is half-aggregated or enzymatically dead is a common and expensive surprise.
On the reagent side, the same group often generates the antibodies and tool reagents a program needs. That includes custom antibody production by immunization or display, hybridoma development, recombinant antibody expression, fragment generation (Fab, scFv, VHH), and downstream conjugation to fluorophores, biotin, or other labels for use as detection reagents. The strongest vendors also handle the awkward jobs others avoid: difficult membrane proteins, large complexes, isotope-labeled protein for NMR, and milligram-to-gram scale-ups when a screening campaign or animal study needs more material than a single prep yields.
The deciding factor is rarely price. It is whether this group can make your specific protein well, at the quality and quantity your downstream work needs, on a timeline that does not stall the program. A vendor that excels at soluble E. coli enzymes may struggle with a glycosylated receptor or a seven-transmembrane target, so match the shop to the protein in front of you before you compare quotes. Ask for relevant case studies in your protein class and expression system, and confirm the people who would run your project have actually made something like it.
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