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Biochemicals

Tetrodotoxin, Na+ channel blocker (ab120054)

Price and availability

134 016 ₸

Availability

Order now and get it on Thursday February 25, 2021

Tetrodotoxin, Na<sup>+</sup> channel blocker (ab120054)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Na+ channel blocker
  • CAS Number: 4368-28-9
  • Purity: > 98%
  • Soluble in pH 4.8 citrate buffer to 100 mM
  • Form / State: Solid
  • Source: Fugu

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Overview

  • Product name

    Tetrodotoxin, Na+ channel blocker
  • Description

    Na+ channel blocker
  • Alternative names

    • TTX
  • Biological description

    Potent, selective and reversible, use-dependent inhibitor of voltage-dependent Na+ channels.

  • Purity

    > 98%
  • General notes

    To purchase this product, additional information may be required for security reasons. Please contact customer services for further details.

  • CAS Number

    4368-28-9
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    Octahydro-12-(hydroxymethyl)-2-imino-5,9:7,10a-dimethano-10aH-[1,3]dioxocino[6,5-d] pyrimidine-4,7,10,11,12-pentol
  • Molecular weight

    319.27
  • Molecular formula

    C11H17N3O8
  • PubChem identifier

    6324668
  • Storage instructions

    Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in pH 4.8 citrate buffer to 100 mM
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Toxic, refer to SDS for further information.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    O[C@H]3C14NC(=N)N[C@H](O)[C@@H]4C2O[C@]3(O)O[C@H](C1O)C2(O)CO
  • Source

    Fugu

  • Research areas

    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Chemical Type
    • Toxin
    • Biochemicals
    • Pharmacology
    • Ion Channels
    • Sodium
    • Blockers
    • Biochemicals
    • Research Area
    • Diabetes
    • Sodium
    • Blockers
    • Biochemicals
    • Research Area
    • Heart disease
    • Sodium
    • Blockers
    • Biochemicals
    • Research Area
    • Hypertension
    • Sodium
    • Blockers
    • Biochemicals
    • Research Area
    • Obesity
    • Sodium
    • Blockers
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Sodium
    • Blockers
    • Biochemicals
    • Research Area
    • Respiratory disease
    • Sodium
    • Blockers
    • Biochemicals
    • Research Area
    • Stroke
    • Sodium
    • Blockers

Images

  • Functional Studies - Tetrodotoxin, Na+ channel blocker (ab120054)
    Functional Studies - Tetrodotoxin, Na+ channel blocker (ab120054) Image from Gómez-Gonzalo M et al., PLoS Biol. 2010;8(4):e1000352. Fig 4(E).; doi: 10.1371/journal.pbio.1000352. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/
    TTX blocked the ictal discharge in both field A and B neurons, but not the direct response of field A neurons to a double NMDA pulse (black arrowheads).
  • Functional Studies - Tetrodotoxin, Na+ channel blocker (ab120054)
    Functional Studies - Tetrodotoxin, Na+ channel blocker (ab120054) Image from Riebe I et al., BMC Neuroscience. 2012;13:14. Fig 1.; doi: 10.1186/1471-2202-13-14. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/2.0
    Multiple connections between CA3 and CA1 pyramidal cells and GABAergic cells and CA1 pyramidal cells in young adult rats. (A1) A typical recording at -80 mV from a pyramidal cell, upper trace shows AMPA sEPSCs under control conditions and lower trace shows mEPSCs after wash-in of TTX. (A2) TTX reduces the AMPA EPSC amplitude by 5.9 ± 0.8 pA (P = 0.004, n = 8, two-tailed paired t-test). (A3) TTX reduces AMPA EPSC frequency by 1.5 ± 0.4 Hz (P

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