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DNase I RNase & Protease free

40 Cited Publications
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Based on 40 publication(s) in Google Scholar

DNase I is an enzyme that degrades DNA. DNase I is mainly produced by digestive system organs, such as the pancreas and parotid gland. Three types of DNase I are known in mammals: pancreatic type, parotid type, and pancreatico-parotid type. DNase I plays a key role in the cleavage of extracellular DNA, and is critical for limiting inflammatory responses and maintaining homeostasis. DNase I is responsible for digesting extracellular nucleoproteins, which may be essential for preventing autoimmune responses. Decreased DNase I activity may be associated with the onset and progression of systemic lupus erythematosus (SLE). DNase I (RNase & Protease free) is a molecular biology-grade DNase I purified by chromatography to remove RNase and protease.

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  • DNase I RNase & Protease free Chemical Structure
    DNase I RNase & Protease free Chemical Structure
  • Experimental Validation Results for DNase I RNase & Protease free
  • Experimental Validation Results for DNase I RNase & Protease free
  • Experimental Validation Results for DNase I RNase & Protease free
  • Experimental Validation Results for DNase I RNase & Protease free
  • Experimental Validation Results for DNase I RNase & Protease free
  • Experimental Validation Results for DNase I RNase & Protease free
CAS No.: 9003-98-9
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Histological Imaging/StainingWBCell Imaging/StainingIFCell Migration/Invasion Assay
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  • DNase I RNase & Protease free Chemical Structure
    DNase I RNase & Protease free Chemical Structure
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    DNase I RNase & Protease free purchased from MedChemExpress. Usage Cited in: Research (Wash D C). 2025 May 30:8:0705. [Abstract]

    Customer Validation
     Masson staining was conducted to detect fibrosis in tissue samples from different groups. Sham: 3.29% ± 0.64%, MIRI: 30.28% ± 5.87%, MIRI + DNase I: 15.91% ±2.92%, MIRI + GSK484: 17.12% ± 2.48%.

  • 1/16

    DNase I RNase & Protease free purchased from MedChemExpress. Usage Cited in: Research (Wash D C). 2025 May 30:8:0705. [Abstract]

    Customer Validation
     IF was performed to detect the expression of VE-cadherin of HUVECs under different treatments. Neutrophils/Sham: 136.08 ± 20.98, Neutrophils/MIRI: 69.45 ± 8.91, Neutrophils/MIRI + DNase I: 108.14 ± 12.38, Neutrophils/MIRI + GSK484: 111.44 ± 16.16.

  • 1/16

    DNase I RNase & Protease free purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2024 Sep 5;10(1):395. [Abstract]

    Customer Validation
     The whole aorta was detected by western blot, and the expressionof NETs products (ELANE, MPO) was quantitatively analyzed treatd with DNase I (4 mg/kg, intraperitoneally daily for 3 weeks).

  • 1/16

    DNase I RNase & Protease free purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2024 May 2;10(1):214. [Abstract]

    Customer Validation
     The effect of NETs on the proliferation of Cal27 cells was detected by EdU proliferation assay DNase I (1 μg/mL,37°C, 15 min).

  • 1/16

    DNase I RNase & Protease free purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2024 May 2;10(1):214. [Abstract]

    Customer Validation
     The effect of NETs on the invasion of Cal27 cells was detected by Transwell invasion assay DNase I (1 μg/mL,37°C, 15 min).

  • 1/16

    DNase I RNase & Protease free purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2024 May 2;10(1):214. [Abstract]

    Customer Validation
     The effect of NETs on the migration of Cal27 cells was detected by wound healing assay treated with DNase I (1 μg/mL,37°C, 15 min).

  • DNase I RNase & Protease free