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human lon protease rabbit antisera  (Bio-Rad)


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    Bio-Rad human lon protease rabbit antisera
    Fig. 1. Validation of the data obtained by microarray analysis on adipose tissue from lipodystrophy patients. (a) Differences in transcription levels of the indicated genes between adipose tissue from lipodystrophy patients and controls, as evaluated by real- time PCR. (b) Representative western blot of <t>LON</t> <t>protease</t> expression in adipose tissue from lipodystrophy patients and healthy controls. (c) Quantitative data, based upon densitometric analysis of all samples, are reported in the histogram, setting arbitrarily the first negative control as 1. P < 0.05, P < 0.01. C, control; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; LD, lipodystrophy patients.
    Human Lon Protease Rabbit Antisera, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1906 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+lon+protease+rabbit+antisera/10__1097_slash_qad__0b013e32833779a3-63-9-41?v=Bio-Rad
    Average 96 stars, based on 1906 article reviews
    human lon protease rabbit antisera - by Bioz Stars, 2026-08
    96/100 stars

    Images

    1) Product Images from "Upregulation of nuclear-encoded mitochondrial LON protease in HAART-treated HIV-positive patients with lipodystrophy: implications for the pathogenesis of the disease"

    Article Title: Upregulation of nuclear-encoded mitochondrial LON protease in HAART-treated HIV-positive patients with lipodystrophy: implications for the pathogenesis of the disease

    Journal: AIDS

    doi: 10.1097/qad.0b013e32833779a3

    Fig. 1. Validation of the data obtained by microarray analysis on adipose tissue from lipodystrophy patients. (a) Differences in transcription levels of the indicated genes between adipose tissue from lipodystrophy patients and controls, as evaluated by real- time PCR. (b) Representative western blot of LON protease expression in adipose tissue from lipodystrophy patients and healthy controls. (c) Quantitative data, based upon densitometric analysis of all samples, are reported in the histogram, setting arbitrarily the first negative control as 1. P < 0.05, P < 0.01. C, control; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; LD, lipodystrophy patients.
    Figure Legend Snippet: Fig. 1. Validation of the data obtained by microarray analysis on adipose tissue from lipodystrophy patients. (a) Differences in transcription levels of the indicated genes between adipose tissue from lipodystrophy patients and controls, as evaluated by real- time PCR. (b) Representative western blot of LON protease expression in adipose tissue from lipodystrophy patients and healthy controls. (c) Quantitative data, based upon densitometric analysis of all samples, are reported in the histogram, setting arbitrarily the first negative control as 1. P < 0.05, P < 0.01. C, control; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; LD, lipodystrophy patients.

    Techniques Used: Biomarker Discovery, Microarray, Real-time Polymerase Chain Reaction, Western Blot, Expressing, Negative Control, Control



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    Bio-Rad human lon protease rabbit antisera
    Fig. 1. Validation of the data obtained by microarray analysis on adipose tissue from lipodystrophy patients. (a) Differences in transcription levels of the indicated genes between adipose tissue from lipodystrophy patients and controls, as evaluated by real- time PCR. (b) Representative western blot of <t>LON</t> <t>protease</t> expression in adipose tissue from lipodystrophy patients and healthy controls. (c) Quantitative data, based upon densitometric analysis of all samples, are reported in the histogram, setting arbitrarily the first negative control as 1. P < 0.05, P < 0.01. C, control; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; LD, lipodystrophy patients.
    Human Lon Protease Rabbit Antisera, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+lon+protease+rabbit+antisera/10__1097_slash_qad__0b013e32833779a3-63-9-41?v=Bio-Rad
    Average 96 stars, based on 1 article reviews
    human lon protease rabbit antisera - by Bioz Stars, 2026-08
    96/100 stars
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    Fig. 1. Validation of the data obtained by microarray analysis on adipose tissue from lipodystrophy patients. (a) Differences in transcription levels of the indicated genes between adipose tissue from lipodystrophy patients and controls, as evaluated by real- time PCR. (b) Representative western blot of LON protease expression in adipose tissue from lipodystrophy patients and healthy controls. (c) Quantitative data, based upon densitometric analysis of all samples, are reported in the histogram, setting arbitrarily the first negative control as 1. P < 0.05, P < 0.01. C, control; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; LD, lipodystrophy patients.

    Journal: AIDS

    Article Title: Upregulation of nuclear-encoded mitochondrial LON protease in HAART-treated HIV-positive patients with lipodystrophy: implications for the pathogenesis of the disease

    doi: 10.1097/qad.0b013e32833779a3

    Figure Lengend Snippet: Fig. 1. Validation of the data obtained by microarray analysis on adipose tissue from lipodystrophy patients. (a) Differences in transcription levels of the indicated genes between adipose tissue from lipodystrophy patients and controls, as evaluated by real- time PCR. (b) Representative western blot of LON protease expression in adipose tissue from lipodystrophy patients and healthy controls. (c) Quantitative data, based upon densitometric analysis of all samples, are reported in the histogram, setting arbitrarily the first negative control as 1. P < 0.05, P < 0.01. C, control; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; LD, lipodystrophy patients.

    Article Snippet: The membrane was incubated in the presence of a human LON protease rabbit antisera (a kind gift from Dr K. Suzuki, University of New Jersey, New Jersey, USA), washed and incubated with an anti-rabbit secondary antibody conjugated to horseradish peroxidase (HRP; Serotec, Kidlington, UK).

    Techniques: Biomarker Discovery, Microarray, Real-time Polymerase Chain Reaction, Western Blot, Expressing, Negative Control, Control