Puromycin 2HCl

Catalog No.S7417 Batch:S741711

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Technical Data

Formula

C22H29N7O5.2HCl

Molecular Weight 544.43 CAS No. 58-58-2
Solubility (25°C)* In vitro DMSO 100 mg/mL (183.67 mM)
Water 100 mg/mL (183.67 mM)
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

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Biological Activity

Description Puromycin 2HCl is an aminonucleoside antibiotic derived from Streptomyces alboniger. It is an inhibitor of protein synthesis and has been used to study transcription regulatory mechanisms that control the sequential and coordinated expression of genes during cell differentiation.
In vitro

The antibiotic puromycin is produced by the actinoniycete, Streptornyces alboniger, and has been used as a tool for studying protein synthesis in a number of systems. [1]

Puromycin can be used for the selection of recombinant cells from noncultured cells. [2]

In vivo

Puromycin (aminonucleoside) inhibits protein synthesis leading to proteinuria & glomerulosclerosis/nephrosis.[4]

Protocol (from reference)

Cell Assay:

[3]

  • Cell lines

    HepG2 cells 

  • Concentrations

    1.6 μM

  • Incubation Time

    72 h

  • Method

    Cells were treated with different concentrations of drug for 72 h.

Animal Study:

[4]

  • Animal Models

    Male Sprague-Dawley rats

  • Dosages

    5 mg/100 g

  • Administration

    i.v.

Selleck's Puromycin 2HCl has been cited by 168 publications

Suppression of ITPKB degradation by Trim25 confers TMZ resistance in glioblastoma through ROS homeostasis [ Signal Transduct Target Ther, 2024, 9(1):58] PubMed: 38438346
The dopamine receptor D1 inhibitor, SKF83566, suppresses GBM stemness and invasion through the DRD1-c-Myc-UHRF1 interactions [ J Exp Clin Cancer Res, 2024, 43(1):25] PubMed: 38246990
Hyperactivation of β-catenin signal in hepatocellular carcinoma recruits myeloid-derived suppressor cells through PF4-CXCR3 axis [ Cancer Lett, 2024, 586:216690] PubMed: 38307410
DHCR7 promotes lymph node metastasis in cervical cancer through cholesterol reprogramming-mediated activation of the KANK4/PI3K/AKT axis and VEGF-C secretion [ Cancer Lett, 2024, 584:216609] PubMed: 38211648
SHMT2 promotes papillary thyroid cancer metastasis through epigenetic activation of AKT signaling [ Cell Death Dis, 2024, 15(1):87] PubMed: 38272883
MDM2 provides TOP2 poison resistance by promoting proteolysis of TOP2βcc in a p53-independent manner [ Cell Death Dis, 2024, 15(1):83] PubMed: 38263255
METTL3 facilitates renal cell carcinoma progression by PLOD2 m6A-methylation under prolonged hypoxia [ Cell Death Dis, 2024, 15(1):62] PubMed: 38233403
Protein phosphatase 1 regulatory subunit 15 A promotes translation initiation and induces G2M phase arrest during cuproptosis in cancers [ Cell Death Dis, 2024, 15(2):149] PubMed: 38365764
Dual roles of CCDC102A in governing centrosome duplication and cohesion [ Cell Rep, 2024, 43(2):113696] PubMed: 38280197
EP300-ZNF384 transactivates IL3RA to promote the progression of B-cell acute lymphoblastic leukemia [ Cell Commun Signal, 2024, 22(1):211] PubMed: 38566191

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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.

NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.