Peptide Medix product catalog

Peptide Medix

Botulinum Toxin Type A — Prescription Reference

Clostridial neurotoxin, SNAP-25 protease — prescription-only reference listing

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Overview

The active substance is botulinum neurotoxin serotype A, produced by the anaerobic bacterium Clostridium botulinum. The purified neurotoxin is a roughly 150 kDa dichain protein: a 100 kDa heavy chain responsible for neuronal binding and translocation, disulfide-linked to a 50 kDa light chain that is a zinc-dependent endopeptidase. In most commercial presentations the neurotoxin is associated with non-toxic accessory proteins in a larger complex, although a purified complex-free formulation also exists.

A point that matters for identification: potency is expressed in Units defined by each manufacturer's own mouse assay, so Units are product-specific and are not interchangeable between brands. The 50 U and 100 U presentations listed here are reference descriptions of vial strength only. Listed for reference.

Specifications

Brand Peptide Medix
Category Aesthetic Biologics
Regulatory status Prescription-only biologic medicine (Rx); supplied solely against valid prescription or institutional authorisation
Active substance Botulinum neurotoxin type A (BoNT/A)
Source organism Clostridium botulinum, anaerobic culture and purification
CAS number 93384-43-1
Molecular weight ≈150 kDa neurotoxin; commonly supplied as a ~900 kDa complex with non-toxic accessory proteins, or complex-free
Structure Dichain protein — 100 kDa heavy chain and 50 kDa light chain joined by an interchain disulfide bond
Molecular target SNAP-25, cleaved by the zinc-dependent endopeptidase light chain
Pharmacological effect Blocks calcium-dependent acetylcholine release at cholinergic nerve terminals
Potency units Units defined by a manufacturer-specific mouse LD50 assay; not interchangeable between products
Form Sterile vacuum-dried or lyophilised powder in a single-use glass vial, reconstituted before use
Reference sizes listed 50 U vial; 100 U vial
Storage Cold chain per approved labelling — unopened vials refrigerated at 2–8 °C (some presentations frozen); reconstituted product refrigerated and used within the labelled window
Intended use Reference listing only — prescription medicine, administered exclusively by qualified clinicians
SKU BOTULINUM-TOXIN-50-U-VIAL

Highlights

  • Prescription-only biologic administered by qualified clinicians — listed here for reference only
  • Botulinum neurotoxin serotype A from Clostridium botulinum; CAS 93384-43-1
  • 150 kDa dichain protein: 100 kDa binding/translocation heavy chain, 50 kDa catalytic light chain
  • Light chain is a zinc endopeptidase that cleaves SNAP-25, blocking acetylcholine release
  • Units are manufacturer-specific and not interchangeable between products
  • Cold-chain product; labelling carries a boxed warning on distant spread of toxin effect

What's Included

  • The vial option and size selected above
  • Final item and quantity confirmed in cart
  • Laboratory-research-use labeling

Research Overview

Molecule and manufacture

Mechanism of action

Action is a four-step sequence. The heavy chain C-terminal domain binds ganglioside and protein receptors — for type A, SV2 — on cholinergic nerve terminals. The toxin is internalised by endocytosis; acidification of the vesicle drives the heavy chain N-terminal domain to form a channel through which the light chain translocates into the cytosol. There the light chain, a zinc metalloprotease, cleaves SNAP-25, a SNARE protein required for vesicle fusion. Without intact SNAP-25 the terminal cannot release acetylcholine, and transmission at the neuromuscular junction or at autonomic cholinergic synapses is interrupted until the terminal regenerates.

Approved indications as a public regulatory fact

  • Cervical dystonia, blepharospasm and strabismus
  • Upper and lower limb spasticity in adults and paediatric patients
  • Prophylaxis of headaches in adults with chronic migraine
  • Severe primary axillary hyperhidrosis inadequately managed by topical agents
  • Overactive bladder and detrusor overactivity associated with a neurologic condition
  • Temporary improvement in the appearance of glabellar, lateral canthal and forehead lines

Regulatory and biosecurity context

Botulinum Toxin Type A — Prescription Reference FAQ

Is botulinum toxin available without a prescription?
No. It is a prescription-only biologic that must be administered by a qualified clinician, and in the United States the neurotoxin is additionally a regulated select agent above defined amounts. This page is a reference listing; product is supplied only against a valid prescription or documented institutional authorisation.
How does it stop muscle contraction?
The heavy chain binds SV2 and ganglioside receptors on cholinergic nerve terminals and the toxin is endocytosed. Vesicle acidification translocates the light chain into the cytosol, where this zinc endopeptidase cleaves SNAP-25. Without intact SNAP-25 the SNARE complex cannot fuse vesicles, so acetylcholine release is blocked.
Are Units the same across different brands?
No. Potency Units are defined by each manufacturer's own mouse assay, so a Unit of one product is not equivalent to a Unit of another. Approved labelling states explicitly that Units cannot be converted or compared between botulinum toxin products, which is why brand identity always accompanies a Unit figure.

This catalog listing is for laboratory research use only. It is not represented as a drug, food, supplement, cosmetic or diagnostic product, and it is not offered for human or veterinary use.

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