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Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
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Gly-Pro-AMC hydrobromide is a fluorescent dye that serves as a specific fluorescent substrate for detecting Dipeptidyl peptidase IV (DPP-IV) activity. It is intended for research use only.
Fluorescent dye
Specific fluorescent substrate for detecting Dipeptidyl peptidase IV (DPP-IV) activity
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Luciferin is a common bioluminescent reporter used for in vivo imaging of the expression of luciferase. This water soluble substrate for the firefly luciferase enzyme utilizes ATP and Mg2+ as cofactors to emit a characteristic yellow-green emission in the presence of oxygen, which shifts to red light in vivoat 37°C. Through the utilization of ATP, the reaction can be further used to indicate the presence of energy or life in order to function as a life-death stain.
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This item MFG by HYPHEN BioMed and Dis. by Aniara Diagnostics. Chromogenic substrate for thrombin, lyophilized. Peptide sequence H-D-Phe-Pip-Arg-pNa, 2HCl. 12 vials x 25 mg.
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Coelenterazines are luminescent enzyme substrates for apoaequorin and Renilla luciferase. Apoaequorin is used as a calcium indicator whereas Renilla luciferase is commonly used as a reporter of transcription regulation. Coelenterazine binds apoaequorin to form an aequorin complex which emits light upon calcium binding, and can measure a broad range of calcium concentrations from ~0.1 uM to >100 uM. Renilla luciferase is widely used as a reporter protein and as a donor in bioluminescence resonance energy transfer (BRET) to study protein-protein interactions. Coelenterazines can also be used for chemiluminescent detection of superoxide anion and peroxynitrite in cells or tissues.Coelenterazine (native): Yellow solid soluble in MeOH or EtOH; Store at -20°C and protect from light; C26H21N3O3; MW: 423; [55779-48-1]. See also other Coelentrazine analogs and water-soluble Aquaphile™ Coelenterazines (native and analog h) for in vivo use.
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Ac-ANW-AMC is a fluorogenic substrate of the chymotrypsin-like activity of proteasomes. This substrate is preferentially cleaved by immunoproteasomes compared to constitutive 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 chymotrypsin-like activity of immunoproteasomes. Working concentration is 50 - 200 µM.
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The TGFBR1 peptide sequence (KKKVLTQMGSPSIRC-S(pS)VS) is derived from human SMAD3 (215-230) and is suitable for use as the substrate for TGFBR1 superfamily, including ACVRs (ALK1, ALK2, ALK4 and ALK7) and BMPRs (ALK3 and ALK6).
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Recombinant canine HER2 (ERBB2/CD340) protein comprising residues T23-T652 with a C-terminal His tag, produced in HEK293 cells and supplied lyophilized. Supplied as a purified extracellular/truncated form for use in antibody binding studies, assay development, and signaling research. Manufacturer reconstitution and storage guidance should be followed.
Purity greater than 95% by reducing SDS-PAGE.
Expressed in HEK293 cells for native-like glycosylation.
C-terminal His tag facilitates detection and purification.
Lyophilized from PBS (pH 7.4) for improved stability.
Store at -20°C; reconstitute to ≥100 μg/mL and aliquot for long-term storage.
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D-Luciferin (CAS 2591-17-5) is a membrane-permeable bioluminescent substrate for firefly luciferase characterized by a Km of approximately 2 M In the presence of ATP luciferin undergoes oxidation and decarboxylation catalyzed by luciferase emitting measurable photons This bioluminescence enables quantification of intracellular ATP levels both in vitro and in vivo In biomedical research D-Luciferin is commonly applied for monitoring promoter-driven luciferase gene expression and as a non-invasive imaging probe in bioluminescence imaging (BLI) studies to assess tumor burden pharmacodynamics and cellular ATP content
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A fluorogenic HDAC substrate; ex/em = 340-360/440-460 nm, respectively; following deacetylation by an HDAC and trypsin cleavage, AMC is released and its fluorescence can be used to quantify HDAC activity
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