β-Amyloid 22-35

CAS No. 144189-71-9

β-Amyloid 22-35( Amyloid β-Protein (22-35) )

Catalog No. M29924 CAS No. 144189-71-9

β-Amyloid (22-35) is a 14-aa peptide, shows aggregates and induces neurotoxicity in the hippocampal cells. Beta amyloid (22-35) is a synthetic truncated fragment of beta-amyloid peptide.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
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10MG 356 Get Quote
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Biological Information

  • Product Name
    β-Amyloid 22-35
  • Note
    Research use only, not for human use.
  • Brief Description
    β-Amyloid (22-35) is a 14-aa peptide, shows aggregates and induces neurotoxicity in the hippocampal cells. Beta amyloid (22-35) is a synthetic truncated fragment of beta-amyloid peptide.
  • Description
    β-Amyloid (22-35) is a 14-aa peptide, shows aggregates and induces neurotoxicity in the hippocampal cells. Beta amyloid (22-35) is a synthetic truncated fragment of beta-amyloid peptide. (In Vitro):β-Amyloid (22-35) shows significant cytotoxicity on the rat hippocampal neurons at 40 μg/mL, but exhibits no cytotoxic effect on the glial cells.
  • In Vitro
    β-Amyloid 22-35 shows significant cytotoxicity on the rat hippocampal neurons at 40 μg/mL, but exhibits no cytotoxic effect on the glial cells.
  • In Vivo
    ——
  • Synonyms
    Amyloid β-Protein (22-35)
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Beta Amyloid
  • Recptor
    Amyloid-β
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    144189-71-9
  • Formula Weight
    1403.62
  • Molecular Formula
    C59H102N16O21S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 1.85 mg/mL (1.32 mMu)
  • SMILES
    ——
  • Chemical Name
    Sequence:Glu-Asp-Val-Gly-Ser-Asn-Lys-Gly-Ala-Ile-Ile-Gly-Leu-Met

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

Takadera T, et al. Toxic effect of a beta-amyloid peptide (beta 22-35) on the hippocampal neuron and its prevention. Neurosci Lett. 1993 Oct 14;161(1):41-4.
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