Name: Botulinum Neurotoxin (BoNT) B Substrate Modification (amide) - FITC labeled
Brand: Molecular Depot
SKU: B2019512
Price: 895.00 USD
Availability: InStock

<h2>What are peptide-carrier protein conjugates?</h2>
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Peptide-carrier protein conjugates are synthetic peptides chemically coupled to a larger immunogenic carrier protein, most commonly keyhole limpet hemocyanin (KLH), bovine serum albumin (BSA), or ovalbumin (OVA), addressing the fact that a short peptide antigen is often too small on its own to stimulate a strong immune response during immunization. The carrier protein contains many additional epitopes that help stimulate T-cell and B-cell responses, with KLH generally offering the highest immunogenicity of the common options.
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<h2 dir="ltr">What you will find:</h2>
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Carrier-Linked Immunogens: Specialized sequences chemically bound to macromolecular carriers to enhance immunogenicity and stimulate robust antibody production.
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Labeled Tracking Complexes: High-stability peptide chains coupled with functional groups or dyes to enable clear localization and precise visualization within cellular systems.
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Targeted Transport Ligands: Engineered molecular constructs configured to facilitate directional cross-membrane delivery and specific receptor interactions.
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<h2>How to choose a peptide-carrier protein conjugate</h2>
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Choose KLH as the default carrier for highest immunogenicity
KLH is the most frequently used carrier protein for peptide conjugates specifically because of its high immunogenicity relative to other common carrier options, and it does not interfere with subsequent ELISA or western blot experiments since it isn't typically used as a blocking reagent in those assays.
Use OVA as a control carrier to verify antibody specificity
Conjugating the same peptide to ovalbumin instead of KLH or BSA, then testing the resulting antiserum against both conjugates, helps verify that an antibody raised against a KLH or BSA conjugate is actually specific to the peptide itself rather than to the carrier protein.
Confirm your coupling chemistry matches your peptide's added residue
Thiol-maleimide chemistry is the most common, highly specific coupling method, requiring a cysteine residue on the peptide, while glutaraldehyde coupling works through free amino groups and carbodiimide (EDC/WSC) chemistry couples through free carboxyl groups, each suited to a different peptide modification.
Decide on conjugation site based on which terminus carries your target epitope
If the natural epitope sits at one terminus of the peptide, the added conjugation residue, commonly cysteine, should generally be placed at the opposite terminus to avoid disrupting the antigenic region during coupling to the carrier.
Confirm conjugation efficiency and purity before proceeding to immunization
A well-executed peptide-carrier conjugation should achieve high peptide yield with low levels of unconjugated peptide remaining, and confirming this through methods like SDS-PAGE or mass spectrometry analysis helps ensure a quality immunogen before committing to an immunization schedule.
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<h2>Specifications context</h2>
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KLH ranges in molecular weight from approximately 4.5x10^5 to over 1x10^7 daltons depending on its aggregation state, making it substantially larger than BSA or OVA and contributing to its comparatively higher immunogenicity as a carrier protein for peptide conjugation. As of 2026, thiol-maleimide coupling chemistry, using a peptide engineered with an added terminal cysteine, remains the most widely used and reliable method for peptide-to-carrier conjugation across custom antibody production services.
<a href="https://mbpinc.net/contact-us" style="color: #236fa1; text-decoration: underline;">Contact the helpful team</a> at MBP today to request a quote.

Peptide Conjugates

Molecular Depot

Key Specifications

Botulinum Neurotoxin (BoNT) B Substrate Modification (amide) - FITC labeled

Botulinum Neurotoxin (BoNT) B Substrate Modification (amide) - FITC labeled, catalog B2019512, is a synaptobrevin (VAMP2)-derived substrate peptide for botulinum neurotoxin type B, labeled with FITC (fluorescein) via an aminohexanoyl (LC) linker, with typical uses including BoNT/B protease activity assays. Available from MBP, a registered vendor at leading US research institutions.