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50032

Fluorogenic HDAC/SIRT substrate 1

BPS Bioscience

DESCRIPTION

A fluorogenic, acetylated peptide substrate for HDAC2, HDAC3, and HDAC6 (tested so far). This substrate fluoresces at excitation 350-380 nm, emission at 440-460 nm. It should be used in conjunction with HDAC Developer, Cat. # 50030.

DETAILS

  • Tags: AMC
  • Format: DMSO solution
  • Shiptemp: -20°C or -80°C
  • Warnings: Protect from direct exposure to light. Avoid freeze/thaw cycles.
  • Category: Deacetylase/Substrates
  • References: 1. A. Ito et al. (2001) EMBO J. 20 1331. 2. A. Ito et al. (2002) EMBO J. 21 6236.3. N.A. Barlev et al. (2001) Mol. Cell 8 1243.
  • Description: A fluorogenic, acetylated peptide substrate for HDAC2, HDAC3, and HDAC6 (tested so far). This substrate fluoresces at excitation 350-380 nm, emission at 440-460 nm. It should be used in conjunction with HDAC Developer, Cat. # 50030.
  • Supplied As: 5 mM DMSO solution (100 µl)
  • Unspsc Code: 41105331
  • Unspsc Name: Protein chemifluorescent detection reagents or kits or substrates
  • Applications: Study enzyme kinetics, and screen small molecule HDAC inhibitors for drug discovery and HTS applications.
  • Product Type: Substrate
  • Biosafety Level: Not applicable (BSL-1)
  • Storage Stability: Stable at least 12 months from date of receipt, when stored as directed
  • Scientific Category: Deacetylase
  • Instructions for Use: Materials : HDAC Assay buffer (BPS catalog #50031) HDAC Assay developer (BPS catalog #50030) Fluorogenic HDAC Substrate (BPS catalog #50032)HDAC2 (0.1 µg/µl) (BPS catalog #50001) or other class 1 or class 2b HDAC enzyme Step 1 : Add the following reagents to a low binding NUNC black plate (VWR catalog #62408-936): HDAC Assay Buffer, 39 µl1 mg/ml BSA, 5 µl 200 µM HDAC substrate, 5 µlHDAC2, 1 µl Incubate at 37°C for 30 min. Step 2 : Stop the reaction by adding 50 µl of HDAC assay developer (undiluted) and incubate the plate at room temperature for 15 min. Step 3 : Read samples in a microtiter-plate reading fluorimeter capable of excitation at 350-380 nm and emission at 440-460 nm. "Blank" value (no enzyme negative control) is subtracted from all other values.