Sulfo-SANPAH Crosslinker

CAS No. 102568-43-4

Sulfo-SANPAH Crosslinker( Sulfo-SANPAH Cross linker | Sulfo-SANPAH Cross-linker )

Catalog No. M28017 CAS No. 102568-43-4

Sulfo-SANPAH Crosslinker is a water-soluble isobisfunctional protein crosslinker.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 207 In Stock
5MG 176 In Stock
10MG 297 In Stock
25MG 502 In Stock
50MG 699 In Stock
100MG 918 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Sulfo-SANPAH Crosslinker
  • Note
    Research use only, not for human use.
  • Brief Description
    Sulfo-SANPAH Crosslinker is a water-soluble isobisfunctional protein crosslinker.
  • Description
    Sulfo-SANPAH Crosslinker is a water-soluble isobisfunctional protein crosslinker.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Sulfo-SANPAH Cross linker | Sulfo-SANPAH Cross-linker
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    PPARγ
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    102568-43-4
  • Formula Weight
    471.42
  • Molecular Formula
    C16H19N6O9S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (265.73 mM)
  • SMILES
    OS(=O)(=O)[N]1(OC(=O)CCCCCNc2ccc(cc2[N+]([O-])=O)N=[N+]=[N-])C(=O)CCC1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Angélica A Amato, et al. GQ-16, a novel peroxisome proliferator-activated receptor γ (PPARγ) ligand, promotes insulin sensitization without weight gain. J Biol Chem. 2012 Aug 10;287(33):28169-79.
molnova catalog
related products
  • Opnurasib

    Opnurasib (JDQ-443) is an orally available and selective and potent covalent KRAS G12C inhibitor with antitumor activity for the study of advanced non-small cell lung cancer.

  • MitoBloCK-11?(MB-11)

    MitoBloCK-11 (MB-11) is a s mall molecule inhibitor of mitochondrial protein import possibly acts through transport protein Seo1, but not Tom70 or Tom20;?inhibits precursor proteins that contain hydrophobic segments, confers growth in media lacking uracil in a specific manner and affects zebrafish development.

  • CRSP-1

    Endogenous central calcitonin (CT) receptor agonist that stimulates cAMP formation at a potency 350-fold greater than CT (ED50 values are 0.2 and 71 nM respectively). Displays no activity at calcitonin-gene related peptide (CGRP) and adrenomedullin receptors. Inhibits formation of multinuclear osteoclasts with similar efficacy to CT in vitro. Suppresses food intake and increases body temperature in free-feeding rats, and significantly decreases plasma calcium levels in vivo.