apo a1 Search Results


96
Assaypro apoa1 elisa kit
Fig. 3. Effects of ZBBu on apoB and <t>apoA1</t> secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.
Apoa1 Elisa Kit, supplied by Assaypro, 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/apo+a1/pm25837921-66-3-9?v=Assaypro
Average 96 stars, based on 1 article reviews
apoa1 elisa kit - by Bioz Stars, 2026-08
96/100 stars
  Buy from Supplier

92
Randox apolipoproteins a1
Fig. 3. Effects of ZBBu on apoB and <t>apoA1</t> secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.
Apolipoproteins A1, supplied by Randox, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pmc04709622-122-41-48?v=Randox
Average 92 stars, based on 1 article reviews
apolipoproteins a1 - by Bioz Stars, 2026-08
92/100 stars
  Buy from Supplier

92
Rockland Immunochemicals goat anti human apoa
Fig. 3. Effects of ZBBu on apoB and <t>apoA1</t> secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.
Goat Anti Human Apoa, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pmc05006797__res___119___751___s002-53-8-13?v=Rockland+Immunochemicals
Average 92 stars, based on 1 article reviews
goat anti human apoa - by Bioz Stars, 2026-08
92/100 stars
  Buy from Supplier

94
Proteintech apoa1
Fig. 3. Effects of ZBBu on apoB and <t>apoA1</t> secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.
Apoa1, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pmc12927977-17-0-2?v=Proteintech
Average 94 stars, based on 1 article reviews
apoa1 - by Bioz Stars, 2026-08
94/100 stars
  Buy from Supplier

90
Cusabio csb e09804rb
Fig. 3. Effects of ZBBu on apoB and <t>apoA1</t> secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.
Csb E09804rb, supplied by Cusabio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/us09944684-260-20-19?v=Cusabio
Average 90 stars, based on 1 article reviews
csb e09804rb - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

90
Aviva Systems mouse anti apolipoprotein a1
Fig. 3. Effects of ZBBu on apoB and <t>apoA1</t> secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.
Mouse Anti Apolipoprotein A1, supplied by Aviva Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/10__1117_slash_1__jbo__17__8__081412-30-16-22?v=Aviva+Systems
Average 90 stars, based on 1 article reviews
mouse anti apolipoprotein a1 - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

92
Proteintech apolipoprotein a1
Exercise-upregulated miR-122-5p was shuttled by extracellular vesicles and derived from the liver. (A) Electron microscopy analysis revealed typical rounded particles (extracellular vesicle, EV) in isolated fractions; (B) Nanoparticle tracking analysis and Western blot analysis of extracellular vesicles isolated from sedentary and exercised mice; (C) Particle concentration in plasma from sedentary and exercised mice; (D) Contents of miR-122-5p in the extracellular vesicle fraction and the supernatant fraction (extracellular vesicle free) isolated from plasma of sedentary and exercised mice; (E) Expression profile of miR-122-5p in different tissues in response to exercise; (F) Expression profile of pre-miR-122-5p in different tissues in response to exercise; (G) Liver-specific knockdown of miR-122-5p by AAV8 carrying antisense miR-122-5p oligomers was used to test whether liver-derived miR-122-5p contributes to exercise-induced angiogenesis; (H) AAV infection downregulated miR-122-5p in the liver, skeletal muscle, heart, and kidney in sedentary mice and blocked the upregulation of miR-122-5p in the liver and skeletal muscle in response to exercise; (I) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in upregulation of miR-122-5p in plasma; (J and K) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of muscle performance as detected by (J) forelimb grip strength and (K) motor coordination; (L) AAV-anti-122 blocked the upregulation of serum VEGF concentration induced by exercise; (M and N) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of angiogenesis as detected by (M) CD31 staining and (N) expression levels of CD31 and VEGF in skeletal muscles. Scale bars: 100 nm (A); 100 μm (M). n = 6. Values are presented as mean ± SEM. Data are analyzed using the unpaired Student t test (C‒F,) and two-way ANOVA followed by unpaired t tests (H‒N). * p < 0.05; ** p < 0.01. AAV = adeno-associated virus; ANOVA = analysis of variance; <t>APOA1</t> = <t>apolipoprotein</t> <t>A1;</t> CD31 = platelet/endothelial cell adhesion molecule-1; DAPI = 4’,6-diamidino-2-phenylindole; Exe = exercise; GM130 = golgi matrix protein 130; NC = negative control; Sed = sedentary; TSG101 = tumor susceptibility 101; VEGF = vascular endothelial growth factor.
Apolipoprotein A1, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pmc09338338-129-11-25?v=Proteintech
Average 92 stars, based on 1 article reviews
apolipoprotein a1 - by Bioz Stars, 2026-08
92/100 stars
  Buy from Supplier

93
OriGene hdl3 subfractions
Exercise-upregulated miR-122-5p was shuttled by extracellular vesicles and derived from the liver. (A) Electron microscopy analysis revealed typical rounded particles (extracellular vesicle, EV) in isolated fractions; (B) Nanoparticle tracking analysis and Western blot analysis of extracellular vesicles isolated from sedentary and exercised mice; (C) Particle concentration in plasma from sedentary and exercised mice; (D) Contents of miR-122-5p in the extracellular vesicle fraction and the supernatant fraction (extracellular vesicle free) isolated from plasma of sedentary and exercised mice; (E) Expression profile of miR-122-5p in different tissues in response to exercise; (F) Expression profile of pre-miR-122-5p in different tissues in response to exercise; (G) Liver-specific knockdown of miR-122-5p by AAV8 carrying antisense miR-122-5p oligomers was used to test whether liver-derived miR-122-5p contributes to exercise-induced angiogenesis; (H) AAV infection downregulated miR-122-5p in the liver, skeletal muscle, heart, and kidney in sedentary mice and blocked the upregulation of miR-122-5p in the liver and skeletal muscle in response to exercise; (I) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in upregulation of miR-122-5p in plasma; (J and K) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of muscle performance as detected by (J) forelimb grip strength and (K) motor coordination; (L) AAV-anti-122 blocked the upregulation of serum VEGF concentration induced by exercise; (M and N) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of angiogenesis as detected by (M) CD31 staining and (N) expression levels of CD31 and VEGF in skeletal muscles. Scale bars: 100 nm (A); 100 μm (M). n = 6. Values are presented as mean ± SEM. Data are analyzed using the unpaired Student t test (C‒F,) and two-way ANOVA followed by unpaired t tests (H‒N). * p < 0.05; ** p < 0.01. AAV = adeno-associated virus; ANOVA = analysis of variance; <t>APOA1</t> = <t>apolipoprotein</t> <t>A1;</t> CD31 = platelet/endothelial cell adhesion molecule-1; DAPI = 4’,6-diamidino-2-phenylindole; Exe = exercise; GM130 = golgi matrix protein 130; NC = negative control; Sed = sedentary; TSG101 = tumor susceptibility 101; VEGF = vascular endothelial growth factor.
Hdl3 Subfractions, supplied by OriGene, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pm17587765-39-11-14?v=OriGene
Average 93 stars, based on 1 article reviews
hdl3 subfractions - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier

95
Chem Impex International dexamethasone dex
Exercise-upregulated miR-122-5p was shuttled by extracellular vesicles and derived from the liver. (A) Electron microscopy analysis revealed typical rounded particles (extracellular vesicle, EV) in isolated fractions; (B) Nanoparticle tracking analysis and Western blot analysis of extracellular vesicles isolated from sedentary and exercised mice; (C) Particle concentration in plasma from sedentary and exercised mice; (D) Contents of miR-122-5p in the extracellular vesicle fraction and the supernatant fraction (extracellular vesicle free) isolated from plasma of sedentary and exercised mice; (E) Expression profile of miR-122-5p in different tissues in response to exercise; (F) Expression profile of pre-miR-122-5p in different tissues in response to exercise; (G) Liver-specific knockdown of miR-122-5p by AAV8 carrying antisense miR-122-5p oligomers was used to test whether liver-derived miR-122-5p contributes to exercise-induced angiogenesis; (H) AAV infection downregulated miR-122-5p in the liver, skeletal muscle, heart, and kidney in sedentary mice and blocked the upregulation of miR-122-5p in the liver and skeletal muscle in response to exercise; (I) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in upregulation of miR-122-5p in plasma; (J and K) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of muscle performance as detected by (J) forelimb grip strength and (K) motor coordination; (L) AAV-anti-122 blocked the upregulation of serum VEGF concentration induced by exercise; (M and N) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of angiogenesis as detected by (M) CD31 staining and (N) expression levels of CD31 and VEGF in skeletal muscles. Scale bars: 100 nm (A); 100 μm (M). n = 6. Values are presented as mean ± SEM. Data are analyzed using the unpaired Student t test (C‒F,) and two-way ANOVA followed by unpaired t tests (H‒N). * p < 0.05; ** p < 0.01. AAV = adeno-associated virus; ANOVA = analysis of variance; <t>APOA1</t> = <t>apolipoprotein</t> <t>A1;</t> CD31 = platelet/endothelial cell adhesion molecule-1; DAPI = 4’,6-diamidino-2-phenylindole; Exe = exercise; GM130 = golgi matrix protein 130; NC = negative control; Sed = sedentary; TSG101 = tumor susceptibility 101; VEGF = vascular endothelial growth factor.
Dexamethasone Dex, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pm37158305-50-29-50?v=Chem+Impex+International
Average 95 stars, based on 1 article reviews
dexamethasone dex - by Bioz Stars, 2026-08
95/100 stars
  Buy from Supplier

90
Cusabio apoa1
CPT values and serum proteins levels in healthy individuals and MOH patients
Apoa1, supplied by Cusabio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pmc06798334-82-42-49?v=Cusabio
Average 90 stars, based on 1 article reviews
apoa1 - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

93
Lee Biosolutions human sp
CPT values and serum proteins levels in healthy individuals and MOH patients
Human Sp, supplied by Lee Biosolutions, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/apo+a1/pmc04178065-107-30-32?v=Lee+Biosolutions
Average 93 stars, based on 1 article reviews
human sp - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier

Image Search Results


Fig. 3. Effects of ZBBu on apoB and apoA1 secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.

Journal: Journal of pharmacological sciences

Article Title: The effects of Zanthoxylum bungeanum extract on lipid metabolism induced by sterols.

doi: 10.1016/j.jphs.2014.12.002

Figure Lengend Snippet: Fig. 3. Effects of ZBBu on apoB and apoA1 secretion. HepG2 cells were pretreated with 0.05 mg/mle0.2 mg/ml ZBBu for 12 h and stimulated with sterols for 24 h. After the treatment, apoB and apoA1 in supernatants were evaluated by ELISA. ZBBu could reverse the increased level of apoB induced by 25OH þ cho (A). And ZBBu promoted the secretion of ApoA1 (B). Data are expressed as ratios to the control without treatment of sterols and presented as means ± SD. The mean of at least 3 independent experiments is shown. $P < 0.05, $$P < 0.01 versus normal group. *P < 0.05, **P < 0.01 versus control group treated with 25OH þ cho. #P < 0.05 compared these two control groups. Ctrl: control. Sim: simvastatin. 25OH: 25-hydroxycholesterol. Cho: cholesterol.

Article Snippet: Human apoB and apoA1 ELISA kit were purchased from Assaypro (MO, USA) and Shanghai Hufeng Biotechnology Company (Shanghai, China) respectively.

Techniques: Enzyme-linked Immunosorbent Assay, Control

Exercise-upregulated miR-122-5p was shuttled by extracellular vesicles and derived from the liver. (A) Electron microscopy analysis revealed typical rounded particles (extracellular vesicle, EV) in isolated fractions; (B) Nanoparticle tracking analysis and Western blot analysis of extracellular vesicles isolated from sedentary and exercised mice; (C) Particle concentration in plasma from sedentary and exercised mice; (D) Contents of miR-122-5p in the extracellular vesicle fraction and the supernatant fraction (extracellular vesicle free) isolated from plasma of sedentary and exercised mice; (E) Expression profile of miR-122-5p in different tissues in response to exercise; (F) Expression profile of pre-miR-122-5p in different tissues in response to exercise; (G) Liver-specific knockdown of miR-122-5p by AAV8 carrying antisense miR-122-5p oligomers was used to test whether liver-derived miR-122-5p contributes to exercise-induced angiogenesis; (H) AAV infection downregulated miR-122-5p in the liver, skeletal muscle, heart, and kidney in sedentary mice and blocked the upregulation of miR-122-5p in the liver and skeletal muscle in response to exercise; (I) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in upregulation of miR-122-5p in plasma; (J and K) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of muscle performance as detected by (J) forelimb grip strength and (K) motor coordination; (L) AAV-anti-122 blocked the upregulation of serum VEGF concentration induced by exercise; (M and N) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of angiogenesis as detected by (M) CD31 staining and (N) expression levels of CD31 and VEGF in skeletal muscles. Scale bars: 100 nm (A); 100 μm (M). n = 6. Values are presented as mean ± SEM. Data are analyzed using the unpaired Student t test (C‒F,) and two-way ANOVA followed by unpaired t tests (H‒N). * p < 0.05; ** p < 0.01. AAV = adeno-associated virus; ANOVA = analysis of variance; APOA1 = apolipoprotein A1; CD31 = platelet/endothelial cell adhesion molecule-1; DAPI = 4’,6-diamidino-2-phenylindole; Exe = exercise; GM130 = golgi matrix protein 130; NC = negative control; Sed = sedentary; TSG101 = tumor susceptibility 101; VEGF = vascular endothelial growth factor.

Journal: Journal of Sport and Health Science

Article Title: Exercise promotes angiogenesis by enhancing endothelial cell fatty acid utilization via liver-derived extracellular vesicle miR-122-5p

doi: 10.1016/j.jshs.2021.09.009

Figure Lengend Snippet: Exercise-upregulated miR-122-5p was shuttled by extracellular vesicles and derived from the liver. (A) Electron microscopy analysis revealed typical rounded particles (extracellular vesicle, EV) in isolated fractions; (B) Nanoparticle tracking analysis and Western blot analysis of extracellular vesicles isolated from sedentary and exercised mice; (C) Particle concentration in plasma from sedentary and exercised mice; (D) Contents of miR-122-5p in the extracellular vesicle fraction and the supernatant fraction (extracellular vesicle free) isolated from plasma of sedentary and exercised mice; (E) Expression profile of miR-122-5p in different tissues in response to exercise; (F) Expression profile of pre-miR-122-5p in different tissues in response to exercise; (G) Liver-specific knockdown of miR-122-5p by AAV8 carrying antisense miR-122-5p oligomers was used to test whether liver-derived miR-122-5p contributes to exercise-induced angiogenesis; (H) AAV infection downregulated miR-122-5p in the liver, skeletal muscle, heart, and kidney in sedentary mice and blocked the upregulation of miR-122-5p in the liver and skeletal muscle in response to exercise; (I) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in upregulation of miR-122-5p in plasma; (J and K) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of muscle performance as detected by (J) forelimb grip strength and (K) motor coordination; (L) AAV-anti-122 blocked the upregulation of serum VEGF concentration induced by exercise; (M and N) Liver-specific knockdown of miR-122-5p abolished the effects of exercise in promotion of angiogenesis as detected by (M) CD31 staining and (N) expression levels of CD31 and VEGF in skeletal muscles. Scale bars: 100 nm (A); 100 μm (M). n = 6. Values are presented as mean ± SEM. Data are analyzed using the unpaired Student t test (C‒F,) and two-way ANOVA followed by unpaired t tests (H‒N). * p < 0.05; ** p < 0.01. AAV = adeno-associated virus; ANOVA = analysis of variance; APOA1 = apolipoprotein A1; CD31 = platelet/endothelial cell adhesion molecule-1; DAPI = 4’,6-diamidino-2-phenylindole; Exe = exercise; GM130 = golgi matrix protein 130; NC = negative control; Sed = sedentary; TSG101 = tumor susceptibility 101; VEGF = vascular endothelial growth factor.

Article Snippet: CD36 (18836), CPT1A (15184), carnitine palmitoyl-transferase 1B (CPT1B; 22170), VEGF (19003), apolipoprotein A1 (APOA1; 14427), and golgi matrix protein 130 (GM130; 11308) were purchased from Proteintech.

Techniques: Derivative Assay, Electron Microscopy, Isolation, Western Blot, Concentration Assay, Clinical Proteomics, Expressing, Knockdown, Infection, Staining, Muscles, Virus, Negative Control

CPT values and serum proteins levels in healthy individuals and MOH patients

Journal: BMC Neurology

Article Title: Exploration of candidate serum biomarkers potentially related to the chronic pain condition in Medication–overuse headache

doi: 10.1186/s12883-019-1469-1

Figure Lengend Snippet: CPT values and serum proteins levels in healthy individuals and MOH patients

Article Snippet: Especially, the expression level of the following proteins was evaluated: L-PGDS (human Prostaglandin D Synthase, Lipocalin-type, ELISA kit, BioVendor, Brno, CZ), VDBP (human Vitamin D-binding protein, ELISA kit, Cusabio Biotech, USA), APOE (human apolipoprotein E, Apo-E, ELISA kit, Cusabio Biotech, USA) and APOA1 (human apolipoprotein A1, Apo-A1, ELISA kit, Cusabio Biotech, USA).

Techniques:

Serum proteins levels in MOH patients, according to the prevalent acute headache medication

Journal: BMC Neurology

Article Title: Exploration of candidate serum biomarkers potentially related to the chronic pain condition in Medication–overuse headache

doi: 10.1186/s12883-019-1469-1

Figure Lengend Snippet: Serum proteins levels in MOH patients, according to the prevalent acute headache medication

Article Snippet: Especially, the expression level of the following proteins was evaluated: L-PGDS (human Prostaglandin D Synthase, Lipocalin-type, ELISA kit, BioVendor, Brno, CZ), VDBP (human Vitamin D-binding protein, ELISA kit, Cusabio Biotech, USA), APOE (human apolipoprotein E, Apo-E, ELISA kit, Cusabio Biotech, USA) and APOA1 (human apolipoprotein A1, Apo-A1, ELISA kit, Cusabio Biotech, USA).

Techniques: