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Merck

S1145

Sigma-Aldrich

CD-1用スクリーンカップ

size 85 mL

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1 EA
¥18,660

¥18,660


出荷予定日2025年6月01日



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1 EA
¥18,660

About This Item

UNSPSCコード:
41161502
NACRES:
NB.22

¥18,660


出荷予定日2025年6月01日


サイズ

85 mL

詳細

Screen cup for CD-1 is a stainless-steel cell dissociation sieve that isdeveloped for the preparation of single-cell suspensions from tissue pieces andto fragment polyacrylamide gels.

アプリケーション

Screen cup for CD-1™ has been used as a sieve:

  • for isolation of mice neural cells[1]
  • in isolation of mice cardiomyocytes[2]
  • for filtering cell suspensions of Araucaria angustifolia embryonic cultures[3]

法的情報

CD-1 is a trademark of Sigma-Aldrich Co. LLC

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Slide 1 of 2

1 of 2

Glutathione improves early somatic embryogenesis in Araucaria angustifolia (Bert) O. Kuntze by alteration in nitric oxide emission
Leila do N, et al.
Plant Science, 195, 80-87 (2012)
Sara Dutton Sackett et al.
Scientific reports, 8(1), 10452-10452 (2018-07-12)
Extracellular matrix (ECM) plays an important developmental role by regulating cell behaviour through structural and biochemical stimulation. Tissue-specific ECM, attained through decellularization, has been proposed in several strategies for tissue and organ replacement. Decellularization of animal pancreata has been reported
Guang Li et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(21), E4288-E4295 (2017-05-12)
Alternative splicing changes the CaV1.2 calcium channel electrophysiological property, but the in vivo significance of such altered channel function is lacking. Structure-function studies of heterologously expressed CaV1.2 channels could not recapitulate channel function in the native milieu of the cardiomyocyte.
Haruta Mogami et al.
Scientific reports, 8(1), 696-696 (2018-01-14)
Preterm premature rupture of membranes (pPROM) is a major cause of preterm birth. Recently, extracellular matrix-directed treatment is applied for wound healing. Here, we used a pregnant mouse model to test the efficacy of collagen type 1 gel for healing
Laurine Legroux et al.
Journal of neuroscience methods, 247, 23-31 (2015-03-31)
Flow cytometry is an efficient and powerful technique to characterize and quantify numerous cells. However, the strengths of this technique have not been widely harnessed in neurosciences due to the critical step of CNS tissue preparation into a single cell

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