US$ 27.47
dsip peptide how to use DSIP – Research Peptide |
Description
Cell-culture (3T3-L1 adipocytes) 5-Amino-1MQ at 30 M strongly reduced 1-MNA levels in mouse fat cells, confirming NNMT inhibition (Neelakantan et al., Biochemical Pharmacology, 2018)

The frequency of B12 injections is determined by your specific needs and health objectives

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KEY DETAILS Sterile, nonpyrogenic water for injection Contains 0.9% benzyl alcohol as a bacteriostatic preservative Suitable for multiple withdrawals from a single vial Standard solvent for reconstituting lyophilized peptide compounds Supplied in a 10mL glass vial with rubber stopper and flip-off cap WHAT RESEARCHERS SHOULD KNOW Bacteriostatic water differs from sterile water the benzyl alcohol preservative allows multi-use Always use proper aseptic technique when withdrawing from the vial Store at room temperature (1530C) before opening Once opened, use within 28 days Do not freeze bacteriostatic water
Third-party certificate of analysis (CoA) verification from an accredited analytical laboratory is the minimum standard for any research compound purchase

Our preclinical services Development of radiolabeled antibodies, peptides, and small molecules Development of fluorescent antibodies, peptides, and small molecules Quality control and purification of labeled antibodies, peptides, and small molecules In vitro cell binding and internalization assay (Lindmo assay, IC50 assay, Scatchard assay) In vitro autoradiography Fluorescence microscopy Immunohistochemical staining Immunofluorescence staining Preparation and ethical approval of protocol for animal experiments In vivo biodistribution in rodents In vivo PET and SPECT imaging in rodents In vivo fluorescence imaging in rodents Ex vivo autoradiography of radiolabeled compounds in excised organs Ex vivo fluorescence imaging of fluorescent compounds in excised organs Our translational services GLP and GMP synthesis of precursors for labeling Design of fluorescent and radiolabeled compounds (and precursors) Radiolabeling of compounds for clinical use (GMP) Fluorescent labeling of compounds for clinical use (GMP) Development, validation, and qualification of quality control assays Preclinical toxicity studies IMPD writing Manufacturing and release of labeled study drugs Our clinical services Clinical trial design for Phase 0, Phase I and Phase II clinical trials Statistical Expertise for Phase 0, Phase I and Phase II clinical trials Preparation of clinical trial documentation for submission to authorities Interaction with regulatory authorities to receive clinical trial approval Preparation of Standard Operating Procedures (SOPs) for clinical trial conduct Preparation of study related documents eCRF development Preparation of Trial Master File Clinical study monitoring Patient recruitment & screening (Total body) PET/CT acquisition SPECT/CT acquisition Image analysis and dosimetry In vivo and ex vivo fluorescence imaging (Serious) Adverse event reporting Data & image analysis, statistics, and reporting (Clinical Study Report) The outcome of first in human studies /PoC study Both Phase 1 and 0 are first in human trials, it just depends on what trial objective you choose
