elisa kit (BioVendor Instruments)


Name:
Phosphorylated Neurofilament H Human ELISA
Description:
Catalog Number:
rd191138300r
Price:
$525
Reactivity:
Human
Applications:
Sandwich ELISA, HRP-labelled antibody
Quantity:
96 wells 1 kit
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Images
1) Product Images from "Enhanced ZAG production by subcutaneous adipose tissue is linked to weight loss in gastrointestinal cancer patients"
Article Title: Enhanced ZAG production by subcutaneous adipose tissue is linked to weight loss in gastrointestinal cancer patients
Journal: British Journal of Cancer
doi: 10.1038/sj.bjc.6606083

Figure Legend Snippet: Zinc-α2-glycoprotein gene and protein expression in adipose tissue of cancer patients. mRNA levels of ZAG ( A ) and leptin ( B ) in subcutaneous adipose tissue of weight-stable ( n =8) and cachectic ( n =17) cancer patients by real-time PCR, expressed as means±s.e.m. Zinc- α 2-glycoprotein protein levels in subcutaneous fat of weight-stable ( n =8) and cachectic ( n =17) cancer patients by ELISA, expressed as means±s.e.m. ( C ) Correlation between ZAG protein and mRNA levels ( D ) in adipose tissue; n =25. * P
Techniques Used: Expressing, Real-time Polymerase Chain Reaction, Enzyme-linked Immunosorbent Assay
2) Product Images from "Increased adipose tissue expression of TLR8 in obese individuals with or without type-2 diabetes: significance in metabolic inflammation"
Article Title: Increased adipose tissue expression of TLR8 in obese individuals with or without type-2 diabetes: significance in metabolic inflammation
Journal: Journal of Inflammation (London, England)
doi: 10.1186/s12950-016-0147-y
![... C-reactive protein (CRP) levels were determined using commercial ELISA kit and following the manufacturer’s recommendations. The representative ... Increased adipose tissue TLR8 gene expression correlates with typical inflammatory markers. The adipose tissue gene expression of TLR8 and signature inflammatory cytokines/chemokines (TNF-α, IL-18, and IL-8) was determined in 49 non-diabetic (ND) and 45 type-2 diabetic (T2D) individuals using quantitative real-time RT-PCR while plasma high-sensitivity C-reactive protein (CRP) levels were determined using commercial ELISA kit and following the manufacturer’s recommendations. The representative data from two independent determinations show that TLR8 mRNA expression was associated with the expression of ( a ) TNF-α [ND] ( r = 0.45, P = 0.001); ( b ) IL-18 [ND] ( r = 0.29, P = 0.04); ( c ) IL-8 [ND] ( r = 0.46, P = 0.001); ( d ) Plasma CRP [ND] ( r = 0.36, P = 0.02); ( e ) TNF-α [T2D] ( r = 0.31, P = 0.04); ( f ) IL-18 [T2D] ( r = 0.53, P = 0.0001); and ( g ) IL-8 [T2D] ( r = 0.47, P = 0.001). ( h ) TLR8 gene expression in T2D patients did not correlate with plasma CRP levels ( r = −0.04, P = 0.81). Due to missing plasma samples, TLR8 correlation with plasma CRP levels is shown for 38 ND and 32 T2D individuals](https://storage.googleapis.com/bioz_article_images/PMC5146894/12950_2016_147_Fig5_HTML.jpg)
Figure Legend Snippet: Increased adipose tissue TLR8 gene expression correlates with typical inflammatory markers. The adipose tissue gene expression of TLR8 and signature inflammatory cytokines/chemokines (TNF-α, IL-18, and IL-8) was determined in 49 non-diabetic (ND) and 45 type-2 diabetic (T2D) individuals using quantitative real-time RT-PCR while plasma high-sensitivity C-reactive protein (CRP) levels were determined using commercial ELISA kit and following the manufacturer’s recommendations. The representative data from two independent determinations show that TLR8 mRNA expression was associated with the expression of ( a ) TNF-α [ND] ( r = 0.45, P = 0.001); ( b ) IL-18 [ND] ( r = 0.29, P = 0.04); ( c ) IL-8 [ND] ( r = 0.46, P = 0.001); ( d ) Plasma CRP [ND] ( r = 0.36, P = 0.02); ( e ) TNF-α [T2D] ( r = 0.31, P = 0.04); ( f ) IL-18 [T2D] ( r = 0.53, P = 0.0001); and ( g ) IL-8 [T2D] ( r = 0.47, P = 0.001). ( h ) TLR8 gene expression in T2D patients did not correlate with plasma CRP levels ( r = −0.04, P = 0.81). Due to missing plasma samples, TLR8 correlation with plasma CRP levels is shown for 38 ND and 32 T2D individuals
Techniques Used: Expressing, Quantitative RT-PCR, Enzyme-linked Immunosorbent Assay
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