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Key Documents

Z370398

Sigma-Aldrich

Carestream® BioMax® light film

Synonyme(s) :

autoradiography film, xray film

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About This Item

Code UNSPSC :
41105341
Nomenclature NACRES :
NB.22

Taille

5 in. (13 cm) × 7 in. (18 cm)

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Description générale

Sheets of film with no interleaved paper
Double-emulsion film on clear base. Provides clearest background and highest sensitivity for chemiluminescence detection systems. Also suitable for autoradiography, but with less sensitivity for high-energy isotopes than X-Omat AR and BioMax MS, and than BioMax MR for medium-energy isotopes.

Informations légales

BioMax is a registered trademark of Carestream Health, Inc.
Carestream is a registered trademark of Carestream Health, Inc.
Kodak is a registered trademark of Eastman Kodak Company

Certificats d'analyse (COA)

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Daye Zhang et al.
Experimental and therapeutic medicine, 19(1), 762-770 (2019-12-20)
Migration and invasion is one of the most important features in tumor metastasis and development. Non-small cell lung cancer (NSCLC) is one of the most common types of cancer globally, and has been linked to air contamination. Evidence indicates that
Jian Zhang et al.
Experimental and therapeutic medicine, 15(4), 3189-3196 (2018-03-17)
Hepatitis B cirrhosis is caused by liver cell necrosis, residual liver cell nodular regeneration, connective tissue hyperplasia and fiber formation, which frequently leads to adrenal insufficiency. Previous reports have demonstrated that human fibroblast growth factor (hFGF)-21 is a multifunctional protein
Jianqiong Zheng et al.
Frontiers in pharmacology, 11, 97-97 (2020-03-19)
Metabolic syndrome is a disorder of energy use and storage, which is characterized by central obesity, dyslipidemia, and raised blood pressure and blood sugar levels. Maternal 25-hydroxyvitamin D deficiency is known to cause metabolic changes, chronic disease, and increased adiposity
Derek W Morris et al.
Human molecular genetics, 23(12), 3316-3326 (2014-01-30)
Identifying rare, highly penetrant risk mutations may be an important step in dissecting the molecular etiology of schizophrenia. We conducted a gene-based analysis of large (>100 kb), rare copy-number variants (CNVs) in the Wellcome Trust Case Control Consortium 2 (WTCCC2)
Steven C Chen et al.
PloS one, 6(5), e19780-e19780 (2011-05-24)
Although recent publications have linked the molecular events driving facioscapulohumeral muscular dystrophy (FSHD) to expression of the double homeobox transcription factor DUX4, overexpression of FRG1 has been proposed as one alternative causal agent as mice overexpressing FRG1 present with muscular
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