densitometry scan quantification Search Results


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Faxitron Bioptics ultrafocus dual energy x ray absorptiometry faxitron quantification
DIO exacerbates phenotypic differences between WT and Fabp4/5 dKO mice. Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10), <t>ultrafocus</t> <t>dual-energy</t> <t>X-ray</t> <t>absorptiometry-Faxitron</t> quantification of total weight (B) and fat weight (C) over the course of HFD administration before tumor cell injection (WT M, n = 9-10; Fabp4/5 dKO M, n = 10; WT F, n = 9-10; Fabp4/5 dKO , n = 10). Glucose levels assessed during glucose (D) and insulin (E) tolerance testing in WT (n = 10) and Fabp4/5 dKO mice (n = 10); statistical analysis performed using 2-way analysis of variance (ANOVA) and Tukey multiple comparisons tests. AUC for glucose tolerance testing (D) and insulin tolerance testing (E); statistical significance was determined using 2-way ANOVA with Tukey multiple comparison tests for panels B-C, whereas unpaired t tests were used for panels D-E (WT, n = 10; Fabp4/5 dKO , n = 10). AUC, area under the curve; min, minute.
Ultrafocus Dual Energy X Ray Absorptiometry Faxitron Quantification, supplied by Faxitron Bioptics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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scanalytics inc master scan gel analysis system
DIO exacerbates phenotypic differences between WT and Fabp4/5 dKO mice. Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10), <t>ultrafocus</t> <t>dual-energy</t> <t>X-ray</t> <t>absorptiometry-Faxitron</t> quantification of total weight (B) and fat weight (C) over the course of HFD administration before tumor cell injection (WT M, n = 9-10; Fabp4/5 dKO M, n = 10; WT F, n = 9-10; Fabp4/5 dKO , n = 10). Glucose levels assessed during glucose (D) and insulin (E) tolerance testing in WT (n = 10) and Fabp4/5 dKO mice (n = 10); statistical analysis performed using 2-way analysis of variance (ANOVA) and Tukey multiple comparisons tests. AUC for glucose tolerance testing (D) and insulin tolerance testing (E); statistical significance was determined using 2-way ANOVA with Tukey multiple comparison tests for panels B-C, whereas unpaired t tests were used for panels D-E (WT, n = 10; Fabp4/5 dKO , n = 10). AUC, area under the curve; min, minute.
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Pharmacia LKB Biotechnology Inc laser densitometer ultro scan xl
DIO exacerbates phenotypic differences between WT and Fabp4/5 dKO mice. Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10), <t>ultrafocus</t> <t>dual-energy</t> <t>X-ray</t> <t>absorptiometry-Faxitron</t> quantification of total weight (B) and fat weight (C) over the course of HFD administration before tumor cell injection (WT M, n = 9-10; Fabp4/5 dKO M, n = 10; WT F, n = 9-10; Fabp4/5 dKO , n = 10). Glucose levels assessed during glucose (D) and insulin (E) tolerance testing in WT (n = 10) and Fabp4/5 dKO mice (n = 10); statistical analysis performed using 2-way analysis of variance (ANOVA) and Tukey multiple comparisons tests. AUC for glucose tolerance testing (D) and insulin tolerance testing (E); statistical significance was determined using 2-way ANOVA with Tukey multiple comparison tests for panels B-C, whereas unpaired t tests were used for panels D-E (WT, n = 10; Fabp4/5 dKO , n = 10). AUC, area under the curve; min, minute.
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Bio-Rad densitometry scan quantification
A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by <t>densitometry</t> and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).
Densitometry Scan Quantification, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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OSTEOSYS CO LTD dual energy x-ray absorptiometry (dexa) scanner
A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by <t>densitometry</t> and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).
Dual Energy X Ray Absorptiometry (Dexa) Scanner, supplied by OSTEOSYS CO LTD, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vilber Lourmat fusion solo stm
A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by <t>densitometry</t> and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).
Fusion Solo Stm, supplied by Vilber Lourmat, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biometra pack version 14 1a27
A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by <t>densitometry</t> and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).
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Molecular Dynamics Inc personal densitometer scan v1 30
A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by <t>densitometry</t> and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).
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Image Search Results


DIO exacerbates phenotypic differences between WT and Fabp4/5 dKO mice. Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10), ultrafocus dual-energy X-ray absorptiometry-Faxitron quantification of total weight (B) and fat weight (C) over the course of HFD administration before tumor cell injection (WT M, n = 9-10; Fabp4/5 dKO M, n = 10; WT F, n = 9-10; Fabp4/5 dKO , n = 10). Glucose levels assessed during glucose (D) and insulin (E) tolerance testing in WT (n = 10) and Fabp4/5 dKO mice (n = 10); statistical analysis performed using 2-way analysis of variance (ANOVA) and Tukey multiple comparisons tests. AUC for glucose tolerance testing (D) and insulin tolerance testing (E); statistical significance was determined using 2-way ANOVA with Tukey multiple comparison tests for panels B-C, whereas unpaired t tests were used for panels D-E (WT, n = 10; Fabp4/5 dKO , n = 10). AUC, area under the curve; min, minute.

Journal: Blood Neoplasia

Article Title: Microenvironmentally derived fatty acid–binding proteins 4 and 5 are novel therapeutic vulnerabilities in multiple myeloma

doi: 10.1016/j.bneo.2026.100229

Figure Lengend Snippet: DIO exacerbates phenotypic differences between WT and Fabp4/5 dKO mice. Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10), ultrafocus dual-energy X-ray absorptiometry-Faxitron quantification of total weight (B) and fat weight (C) over the course of HFD administration before tumor cell injection (WT M, n = 9-10; Fabp4/5 dKO M, n = 10; WT F, n = 9-10; Fabp4/5 dKO , n = 10). Glucose levels assessed during glucose (D) and insulin (E) tolerance testing in WT (n = 10) and Fabp4/5 dKO mice (n = 10); statistical analysis performed using 2-way analysis of variance (ANOVA) and Tukey multiple comparisons tests. AUC for glucose tolerance testing (D) and insulin tolerance testing (E); statistical significance was determined using 2-way ANOVA with Tukey multiple comparison tests for panels B-C, whereas unpaired t tests were used for panels D-E (WT, n = 10; Fabp4/5 dKO , n = 10). AUC, area under the curve; min, minute.

Article Snippet: Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10), ultrafocus dual-energy X-ray absorptiometry-Faxitron quantification of total weight (B) and fat weight (C) over the course of HFD administration before tumor cell injection (WT M, n = 9-10; Fabp4/5 dKO M, n = 10; WT F, n = 9-10; Fabp4/5 dKO , n = 10).

Techniques: Injection, Comparison

A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by densitometry and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).

Journal: PLoS ONE

Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions

doi: 10.1371/journal.pone.0163958

Figure Lengend Snippet: A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by densitometry and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).

Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and densitometry scan quantification (ChemiDoc TM XRS+ System camera and Image Lab TM software, Bio-Rad, Hercules, USA), three molecular species were retained for data processing: native protein (N-HK, 120kDa), light chain (LC-HK, 56kDa), and cleaved light chain (cLC-HK, 46kDa).

Techniques: Purification, Clinical Proteomics, SDS Page, Concentration Assay, MANN-WHITNEY

A : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from nC1Inh-AE male patients (M1 to M5) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by densitometry and N-HK concentration by the displayed linear regression. B, C : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (B) and HK cleavage (C), measured as in panel A, compared to the healthy cohort studied in . D, E, F : as in A, B, C, concerning female patients (W1 to W5). densito: densitometry in 10 7 arbitrary units; ****: p <10 −4 (Mann-Whitney-Wilcoxon test); nC1Inh-AE: angioedema with normal C1 inhibitor.

Journal: PLoS ONE

Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions

doi: 10.1371/journal.pone.0163958

Figure Lengend Snippet: A : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from nC1Inh-AE male patients (M1 to M5) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by densitometry and N-HK concentration by the displayed linear regression. B, C : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (B) and HK cleavage (C), measured as in panel A, compared to the healthy cohort studied in . D, E, F : as in A, B, C, concerning female patients (W1 to W5). densito: densitometry in 10 7 arbitrary units; ****: p <10 −4 (Mann-Whitney-Wilcoxon test); nC1Inh-AE: angioedema with normal C1 inhibitor.

Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and densitometry scan quantification (ChemiDoc TM XRS+ System camera and Image Lab TM software, Bio-Rad, Hercules, USA), three molecular species were retained for data processing: native protein (N-HK, 120kDa), light chain (LC-HK, 56kDa), and cleaved light chain (cLC-HK, 46kDa).

Techniques: Purification, Clinical Proteomics, SDS Page, Concentration Assay, MANN-WHITNEY

High-molecular-weight kininogen (HK) molecular pattern of plasma samples from healthy women taking or not estrogen/progestin combination (OP; Healthy+OP, n = 32; Healthy-OP, n = 30) and from nC1Inh-AE patients taking OP and ≥2 months after OP withdrawal (nC1INh-AE+/-OP, n = 13). A : Analysis of plasma samples (0.5μL/lane) from six patients (O1–O6) and the corresponding figures. N-HK concentration of P1 and P2 was evaluated by the displayed linear regression, kinin-forming activity was determined as in , pathological values were labelled in bold fonts. B, C : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of the plasma concentration of N-HK (B) and cleaved HK species (C), measured as in panel A. D, E : Details of the paired samples of panel B and C respectively analysed using the Wilcoxon matched-pairs signed rank test. densito: densitometry in 10 7 arbitrary units; NS : non-significant; *: p <0.05; **: p <0.01; ***: p <0.001; ****: p <10 −4 (non-parametric tests); N-HK, LC-HK, cLC-HK: native chain, light chain, cleaved light chain of HK respectively; nC1Inh-AE: angioedema with normal C1 inhibitor.

Journal: PLoS ONE

Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions

doi: 10.1371/journal.pone.0163958

Figure Lengend Snippet: High-molecular-weight kininogen (HK) molecular pattern of plasma samples from healthy women taking or not estrogen/progestin combination (OP; Healthy+OP, n = 32; Healthy-OP, n = 30) and from nC1Inh-AE patients taking OP and ≥2 months after OP withdrawal (nC1INh-AE+/-OP, n = 13). A : Analysis of plasma samples (0.5μL/lane) from six patients (O1–O6) and the corresponding figures. N-HK concentration of P1 and P2 was evaluated by the displayed linear regression, kinin-forming activity was determined as in , pathological values were labelled in bold fonts. B, C : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of the plasma concentration of N-HK (B) and cleaved HK species (C), measured as in panel A. D, E : Details of the paired samples of panel B and C respectively analysed using the Wilcoxon matched-pairs signed rank test. densito: densitometry in 10 7 arbitrary units; NS : non-significant; *: p <0.05; **: p <0.01; ***: p <0.001; ****: p <10 −4 (non-parametric tests); N-HK, LC-HK, cLC-HK: native chain, light chain, cleaved light chain of HK respectively; nC1Inh-AE: angioedema with normal C1 inhibitor.

Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and densitometry scan quantification (ChemiDoc TM XRS+ System camera and Image Lab TM software, Bio-Rad, Hercules, USA), three molecular species were retained for data processing: native protein (N-HK, 120kDa), light chain (LC-HK, 56kDa), and cleaved light chain (cLC-HK, 46kDa).

Techniques: High Molecular Weight, Clinical Proteomics, Concentration Assay, Activity Assay

A : High-molecular-weight kininogen (HK) molecular pattern of plasma samples (0.5μL/lane) from two nC1Inh-AE patients (W6, M6) less than 24h after the onset of an AE attack (Att) and at least two weeks after remission (Rem), analysed as in . B : Same as for A, with plasma samples from three patients (K1–K3) with ACEi-AE and low kinin catabolism (L-Cat) and three patients (M7–M9) with nC1Inh-AE and normal kinin catabolism (N-Cat). N-HK concentrations were evaluated by the displayed linear regressions, kinin-forming activity was determined as in , pathological values were labelled in bold font. densito: densitometry in 10 7 arbitrary units; N-HK, LC-HK, cLC-HK: native chain, light chain, cleaved light chain of HK respectively.

Journal: PLoS ONE

Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions

doi: 10.1371/journal.pone.0163958

Figure Lengend Snippet: A : High-molecular-weight kininogen (HK) molecular pattern of plasma samples (0.5μL/lane) from two nC1Inh-AE patients (W6, M6) less than 24h after the onset of an AE attack (Att) and at least two weeks after remission (Rem), analysed as in . B : Same as for A, with plasma samples from three patients (K1–K3) with ACEi-AE and low kinin catabolism (L-Cat) and three patients (M7–M9) with nC1Inh-AE and normal kinin catabolism (N-Cat). N-HK concentrations were evaluated by the displayed linear regressions, kinin-forming activity was determined as in , pathological values were labelled in bold font. densito: densitometry in 10 7 arbitrary units; N-HK, LC-HK, cLC-HK: native chain, light chain, cleaved light chain of HK respectively.

Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and densitometry scan quantification (ChemiDoc TM XRS+ System camera and Image Lab TM software, Bio-Rad, Hercules, USA), three molecular species were retained for data processing: native protein (N-HK, 120kDa), light chain (LC-HK, 56kDa), and cleaved light chain (cLC-HK, 46kDa).

Techniques: High Molecular Weight, Clinical Proteomics, Activity Assay