| Description: | Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. Ac-KQL-AMC is a fluorogenic substrate of the trypsin-like activity of both constitutive and immuno proteasomes. The AMC fluorescence can be detected by a fluorimeter or a plate reader using excitation/emission wavelengths at 360 nm/460 nm, respectively.This substrate can be used to determine the trypsin-like activity of proteasomes. Working concentration is 50 - 200 μM. |
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