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  • The expected molecular weight (MW) listed in the product datasheet is based solely on the size of the target protein’s amino acid sequence. It’s important to remember that many factors can affect the banding pattern of your western blot including: (1) the existence of a splice variant, (2) the quality of the loaded sample, (3) the protein extraction method, and (4) the protein transfer conditions. To achieve accurate results, you may need to systematically adjust the protein extraction method or the protein transfer conditions.

    • If the band’s MW is below the expected MW it could be due to a splice variant with a slightly different MW.
      • Heat the samples at 70°C for 10 min.
      • Increase the transfer time.
    • If the band’s MW is above the expected MW, it could be due to post-translational modifications.
    • In either event, you should use a blocking peptide as a negative control.

  • Some toxins and peptides are soluble in DMSO; you can find this information in the product specification section. For these products, prepare a concentrated stock solution first.

    1. Centrifuge vial (10,000 x g, 5 minutes) before adding solvent.
    2. Dissolve the lyophilized reagent in DMSO. We recommend keeping a concentrated stock solution at 1-10 mM (100-1000X higher than the final working concentration).
    3. Once the peptide is completely dissolved in DMSO, slowly dilute the peptide in pure water (or buffer) to the desired final working concentration.

    Note: We recommend that you maintain a DMSO concentration as low as possible. For cell assays, a final concentration of 0.1–0.5% DMSO (v/v) is considered acceptable. For other experiments, 5% DMSO (v/v) is recommended; adjust this according to your experimental requirements.

  • FAQ 3FAQ 3FAQ 3FAQ 3

Category: Neuroimmunology
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224 Results
  • µ/ω-TRTX-Tap1a
    Bioassay Tested
    µ/ω-TRTX-Tap1a
    A potent blocker/gating-modifier of multiple NaV and T-type (CaV3.1, CaV3.2) channels
    • Product Code: STT-600
    • Applications: Electrophysiology
    • MW: 4182.7 Da
  • Hainantoxin-IV
    Bioassay Tested
    Hainantoxin-IV
    A potent, reversible blocker of neuronal NaV1.7 and other TTX-sensitive voltage-gated sodium channels
    • Product Code: STH-130
    • Applications: Electrophysiology
    • MW: 3987.6 Da
  • Hainantoxin-III
    Bioassay Tested
    Hainantoxin-III
    A potent blocker of neuronal NaV 1.7 and NaV1.2 voltage-gated sodium channels, with activity on NaV1.3 and NaV1.1 subtypes
    • Product Code: STH-120
    • Applications: Electrophysiology
    • MW: 3608 Da
  • mHuwentoxin-IV
    Bioassay Tested
    mHuwentoxin-IV
    A potent and selective blocker of the neuronal NaV1.7 voltage-gated sodium channels
    • Product Code: STH-101
    • Short Description: A potent and selective blocker of the neuronal NaV1.7 voltage-gated sodium channels
    • Applications: Electrophysiology
    • MW: 4088.8 Da
  • Huwentoxin-IV
    Bioassay Tested
    Huwentoxin-IV
    A potent and selective blocker of the neuronal NaV1.7 voltage-gated sodium channels
    • Product Code: STH-100
    • Short Description: A potent and selective blocker of the neuronal NaV1.7 voltage-gated sodium channels
    • Applications: Electrophysiology
    • CAS No.: 526224-73-7
    • MW: 4106.8 Da
  • GsAF-II
    Bioassay Tested
    GsAF-II
    A potent gating modifier of tetrodotoxin-sensitive (TTX-s) neuronal voltage-gated sodium (NaV) channels that also blocks hERG1 potassium channels
    • Product Code: STG-350
    • Short Description: A potent gating modifier of tetrodotoxin-sensitive (TTX-s) neuronal voltage-gated sodium (NaV) channels that also blocks hERG1 potassium channels
    • Applications: Electrophysiology
    • MW: 3979.8 Da
  • GsAF-I
    Bioassay Tested
    GsAF-I
    A potent gating modifier of tetrodotoxin-sensitive (TTX-s) neuronal voltage-gated sodium (NaV) channels that also blocks hERG1 potassium channels
    • Product Code: STG-300
    • Short Description: A potent gating modifier of tetrodotoxin-sensitive (TTX-s) neuronal voltage-gated sodium (NaV) channels that also blocks hERG1 potassium channels
    • Applications: Electrophysiology
    • MW: 3707.5 Da
  • α-Conotoxin PeIA
    Bioassay Tested
    α-Conotoxin PeIA
    An antagonist of neuronal nAChRs (α9α10, α6-containing, and α3/β2) that also inhibits N-type (CaV2.2) calcium channels via GABA(B) receptor activation
    • Product Code: STC-970
    • Applications: Electrophysiology
    • CAS No.: 866876-88-2
    • MW: 1652 Da
  • α-Conotoxin EI
    Bioassay Tested
    α-Conotoxin EI
    A potent and selective antagonist of the muscle-type nicotinic acetylcholine receptor (nAChR)
    • Product Code: STC-900
    • Short Description: A potent and selective antagonist of the muscle-type nicotinic acetylcholine receptor (nAChR)
    • Applications: Electrophysiology
    • CAS No.: 170663-33-9
    • MW: 2093.4 Da
  • α-Conotoxin SI
    Bioassay Tested
    α-Conotoxin SI
    A potent and selective antagonist of the muscle-type nicotinic acetylcholine receptors (nAChRs)
    • Product Code: STC-825
    • Short Description: A potent and selective antagonist of the muscle-type nicotinic acetylcholine receptors (nAChRs)
    • Applications: Electrophysiology
    • CAS No.: 115797-06-3
    • MW: 1353.6 Da
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