1996
DOI: 10.1016/1357-2725(96)00013-1
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Insulin-sensitive glucose transporter transcript levels in calf muscles assessed with a bovine GLUT4 cDNA fragment

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Cited by 18 publications
(33 citation statements)
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“…As in other species, GLUT4 mRNA was detected in the heart, muscles and adipose tissue but not in non insulin-responsive tissues from cattle using either human [100] or bovine cDNA probes [3,49]. Unlike human organs, the liver and kidney of lactating cows express a high GLUT5 mRNA level [100], the physiological role of this transporter still being a matter of conjoncture [70].…”
Section: Immunological Studiesmentioning
confidence: 77%
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“…As in other species, GLUT4 mRNA was detected in the heart, muscles and adipose tissue but not in non insulin-responsive tissues from cattle using either human [100] or bovine cDNA probes [3,49]. Unlike human organs, the liver and kidney of lactating cows express a high GLUT5 mRNA level [100], the physiological role of this transporter still being a matter of conjoncture [70].…”
Section: Immunological Studiesmentioning
confidence: 77%
“…However, many authors have considerable difficulties with this technique, whatever the animal species due to several practical problems. Firstly, some non-specific bands may be detected either with a non-immune serum [96], or even with polyclonal antibodies specifically raised against GLUTs [41,49,85]. Secondly, a confident detection of the GLUT proteins is made difficult because of the inconsistency of their electrophoretic behavior due to the heterogeneity of the protein glycosylation, as for GLUT1 [32,61], GLUT3 [32] and GLUT4 [50,96].…”
Section: Immunological Studiesmentioning
confidence: 99%
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“…The bGHR DNA fragment and a mouse β-cDNA probe (1 kb) were labelled with α[ 32 P]-dCTP (3000 Ci·mmol -1 ) (ICN, France) to a specific activity of 10 8 cpm·µg -1 DNA using a random priming kit (Roche). Used as a control, a rat 18S ribosomal oligonucleotide probe was labelled at the 5'end with γ [ 32 P]-ATP using polynucleotide kinase as described by Hocquette et al [26]. Membranes of muscle mRNA were first hybridised with the 32 P GHR cDNA probe, then they were stripped off (boiling in 0.5% SDS), before re-hybridisation with the 32 P labelled 18S ribosomal oligonucleotide, then with the 32 P β-actin cDNA probe.…”
Section: Northern-blot Analysismentioning
confidence: 99%