Peptide Medix product catalog

ET
Editorial Team
August 16, 2026 5 min read

Cancer research peptides and antibodies in this catalog serve four distinct experimental jobs: they act as checkpoint and receptor ligands in immuno-oncology assays, as angiogenesis modulators, as tumour-marker standards for quantitative immunoassay, and as protease substrates for studying invasion. Our cancer topic page collects the peptide standards, antisera, labeled tracers and kits that laboratories order for that work, grouped by parent molecule. This guide explains which families sit inside the topic, what each is ordered for, and which reagent format fits which question.

What sits under the cancer topic

Inclusion here is by research use, not by any claim about the molecule. A family appears under cancer when its parent protein or peptide is an established target, marker or tool in oncology literature — checkpoint proteins, angiogenesis regulators, gut hormones with documented mitogenic receptors on tumour lines, proteases implicated in matrix degradation, and secreted markers used to stage or track disease in models. Many families are shared with other topics: somatostatin appears in neuropeptide work, adiponectin in obesity studies. Nothing in this section is a therapeutic; every item is supplied for in-vitro and approved animal research only.

Immune checkpoint and immuno-oncology reagents

Checkpoint biology drives a large share of current orders. The relevant families supply blocking peptides, extracellular-domain fragments, and the antisera used to detect expression in tumour tissue:

  • PD-1 and PD-L1 — peptide fragments spanning the interaction interface, used in competition assays, binding studies and as immunogens; antisera for immunohistochemical scoring of tumour sections.
  • CTLA-4 — the second classical checkpoint axis, ordered as peptide standards and antibodies for T-cell co-stimulation work.
  • TNF and interleukin families — cytokine peptides and fragments for tumour-microenvironment studies, and as calibrators for multiplex panels.
  • CXCL and CCL chemokines, plus SDF-1 (CXCL12) — chemotaxis and metastatic-homing assays; SDF-1/CXCR4 is one of the most-studied axes in tumour dissemination.

Angiogenesis and anti-angiogenic peptides

The angiogenesis literature is unusually peptide-rich, because several endogenous inhibitors are proteolytic fragments of larger matrix proteins:

  • Endostatin — the collagen XVIII C-terminal fragment, the archetypal endogenous angiogenesis inhibitor in endothelial migration and tube-formation assays.
  • Anginex — a designed beta-sheet peptide that targets galectin-1 on activated endothelium; a synthetic tool rather than a natural fragment.
  • Vasohibin and PEDF — endothelium-derived negative regulators, ordered as standards and for antibody-based detection.
  • Thrombospondin — the TSP-1 type-1 repeat peptides (including the ABT-510 lineage) are standard positive controls in anti-angiogenic screens.
  • Angiopoietin — Ang-1/Ang-2 and Tie2 pathway reagents for vessel-stability studies, overlapping heavily with the cardiovascular topic.

Tumour markers, growth-factor and invasion families

The remaining families divide between markers measured in samples and mechanistic tools:

  • Chromogranin A — the standard secretory marker for neuroendocrine tumours, and one of the most frequently ordered assay-kit targets in this topic.
  • Gastrin and CCK — CCK-B/gastrin receptor signalling on gastrointestinal tumour lines; ordered as full-length peptides and as receptor-selective analogs.
  • Bombesin and gastrin-releasing peptide — historically important autocrine growth loops in small-cell lung carcinoma models, still used for GRPR-targeted probe development.
  • Somatostatin — SSTR-subtype pharmacology underlies both neuroendocrine tumour imaging and a large body of antiproliferative cell work.
  • Survivin and Bcl family peptides — apoptosis-regulation tools, including BH3-domain peptides used to probe mitochondrial priming.
  • uPAR, cathepsin and autotaxin — the invasion and matrix-remodelling group; cathepsin substrates are usually ordered as fluorogenic labeled peptides.
  • Osteopontin and glypican — adhesion and co-receptor families with established marker roles, glypican-3 particularly in hepatocellular models.
  • TGF-β — context-dependent tumour suppressor and promoter; peptide standards and antisera support both directions of that literature.

Which formats the cancer topic contains

Four product types recur across these families. Synthetic peptide standards are the workhorses: blocking peptides, receptor ligands and immunogens, typically ≥95% HPLC purity in microgram-to-milligram fills. Labeled peptides matter more here than in most topics, because protease assays depend on FRET-paired fluorogenic substrates and because biotinylated ligands drive pull-down work. Polyclonal antisera support immunohistochemistry on tumour sections and Western detection. ELISA and EIA kits quantify secreted markers such as chromogranin A or endostatin in plasma and conditioned medium. Pull-downs and immunoprecipitations additionally use magnetic beads, and epitope-mapping projects use peptide libraries — overlapping scans across a tumour antigen are a routine request.

How laboratories choose within a family

Three decisions dominate. First, fragment versus full-length: checkpoint work almost always uses interface fragments, not the whole ectodomain, and a blocking peptide is validated for absorbing an antibody rather than for receptor pharmacology. Second, species: mouse xenograft and syngeneic models need mouse-sequence reagents, and cross-reactivity of an antiserum raised against the human sequence cannot be assumed — every item states its species reactivity. Third, assay compatibility: a fluorogenic substrate is defined by its label pair and quenching chemistry as much as by its sequence, so check the excitation and emission profile against your plate reader before ordering.

Handling notes for this topic

Most cancer-topic peptides are small, lyophilised and stable for years sealed at −20 °C. Two cautions apply more than usual. Hydrophobic sequences — several BH3 and thrombospondin-derived peptides — dissolve poorly in aqueous buffer and may need an organic co-solvent; see peptide solubility. And fluorogenic substrates are light-sensitive: aliquot under reduced light and store in amber vials. General practice is in the storage guide, the aliquoting guide, and for content verification the COA guide.

Where to go next

Browse the full cancer topic or start from the research catalog hub. Adjacent guides cover the cardiovascular section, which shares the angiogenesis families, and the assay kit type guide if your question is marker quantitation rather than mechanism.

Frequently Asked Questions

Are any of these peptides cancer treatments?
No. Everything in this section is a laboratory reagent supplied for in-vitro assays and approved animal research. Several families — endostatin, thrombospondin fragments, somatostatin analogs — have clinical research histories, but the material in this catalog is not manufactured to pharmaceutical standards and is not for human or veterinary administration under any circumstances.
What is a blocking peptide, and when do I need one?
A blocking peptide is the immunogen sequence an antiserum was raised against. Pre-incubating the antibody with excess blocking peptide should abolish specific staining, which is the standard specificity control for immunohistochemistry and Western blots. It is a control reagent, not a pharmacological tool — see the glossary entry.
Should I order human or mouse sequence reagents for a xenograft study?
It depends on what you are measuring. Human-sequence reagents detect the implanted tumour; mouse-sequence reagents detect host stroma, vasculature and immune infiltrate. Angiogenesis and immune-infiltration readouts in a xenograft are host-derived, so mouse reagents are usually correct there even though the tumour is human.
Why are protease substrates supplied as labeled peptides?
Because activity is read as a fluorescence change. A fluorogenic substrate carries a fluorophore and a quencher flanking the cleavage site; cleavage separates them and signal rises. That design makes the label pair as important as the sequence — match excitation and emission to your instrument. The labeled peptides guide covers the chemistries.
Which cancer-topic markers are best measured with a kit rather than an antibody?
Secreted markers in plasma, serum or conditioned medium — chromogranin A, endostatin, osteopontin, several chemokines. An ELISA or EIA kit bundles a matched antibody pair, standards and a validated range, which is faster and more reproducible than assembling the components. Use antibodies alone for tissue localisation and blotting.
How stable are BH3 and other hydrophobic peptides in solution?
Less stable than typical hydrophilic peptides, and harder to get into solution in the first place. Many require DMSO or another organic co-solvent, then dilution into aqueous buffer, and can aggregate on standing. Prepare fresh where the assay allows, aliquot single-use volumes, and confirm concentration rather than assuming full recovery after filtration.

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