human mbl Search Results


94
Bio-Techne corporation quantikine elisa human mbl immunoassay kit
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Shanghai Korain Biotech Co Ltd masp 2 levels
Serum MBL and <t> MASP-2 levels </t> according to the clinical features of the patients
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Serum MBL and <t> MASP-2 levels </t> according to the clinical features of the patients
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Hycult Biotech human mbl elisa kit
Serum MBL and <t> MASP-2 levels </t> according to the clinical features of the patients
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R&D Systems quantikine elisa kit
Serum MBL and <t> MASP-2 levels </t> according to the clinical features of the patients
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Sino Biological lectin hrmbl
A schematic diagram of quantitative bacteremia identification using opsonin-coated MNPs and μFISH. A) Bacteria in bacteremia blood are magnetically captured and enriched by MNPs conjugated with human recombinant mannose-binding <t>lectin</t> <t>(hrMBL-MNPs).</t> B) The PDMS microfluidic device consists of eight inlets and outlets each for samples and FISH reagents, and 8 dividing channels for high throughput. C) Bacteria captured by the MNPs are magnetically confined in the microfluidic channel and then fixed and permeabilized to hybridize the fluorescence-labeled FISH probes to the complementary 16S rRNA sequences of the target microbes. D) Fluorescent imaging of magnetically captured bacteria ( E. coli : green, S. aureus : magenta).
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R&D Systems duoset elisa
A schematic diagram of quantitative bacteremia identification using opsonin-coated MNPs and μFISH. A) Bacteria in bacteremia blood are magnetically captured and enriched by MNPs conjugated with human recombinant mannose-binding <t>lectin</t> <t>(hrMBL-MNPs).</t> B) The PDMS microfluidic device consists of eight inlets and outlets each for samples and FISH reagents, and 8 dividing channels for high throughput. C) Bacteria captured by the MNPs are magnetically confined in the microfluidic channel and then fixed and permeabilized to hybridize the fluorescence-labeled FISH probes to the complementary 16S rRNA sequences of the target microbes. D) Fluorescent imaging of magnetically captured bacteria ( E. coli : green, S. aureus : magenta).
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R&D Systems human mbl2 quantikine elisa kit
The <t> MBL2 </t> haplotype distribution among treatment naive patients with chronic HBV infection
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R&D Systems biotinylated goat anti human mbl
The <t> MBL2 </t> haplotype distribution among treatment naive patients with chronic HBV infection
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R&D Systems mb mannan
The <t> MBL2 </t> haplotype distribution among treatment naive patients with chronic HBV infection
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Image Search Results


Serum MBL and  MASP-2 levels  according to the clinical features of the patients

Journal: Molecular Biology Reports

Article Title: Association between mannose binding lectin gene polymorphisms and clinical severity of COVID-19 in children

doi: 10.1007/s11033-023-08524-z

Figure Lengend Snippet: Serum MBL and MASP-2 levels according to the clinical features of the patients

Article Snippet: The human MBL and MASP-2 ELISA kits measured serum MBL and MASP-2 levels in samples from patients (BT LAB, China).

Techniques:

Serum MBL and  MASP-2 levels,  according to the Codon 54 polymorphisms

Journal: Molecular Biology Reports

Article Title: Association between mannose binding lectin gene polymorphisms and clinical severity of COVID-19 in children

doi: 10.1007/s11033-023-08524-z

Figure Lengend Snippet: Serum MBL and MASP-2 levels, according to the Codon 54 polymorphisms

Article Snippet: The human MBL and MASP-2 ELISA kits measured serum MBL and MASP-2 levels in samples from patients (BT LAB, China).

Techniques:

A schematic diagram of quantitative bacteremia identification using opsonin-coated MNPs and μFISH. A) Bacteria in bacteremia blood are magnetically captured and enriched by MNPs conjugated with human recombinant mannose-binding lectin (hrMBL-MNPs). B) The PDMS microfluidic device consists of eight inlets and outlets each for samples and FISH reagents, and 8 dividing channels for high throughput. C) Bacteria captured by the MNPs are magnetically confined in the microfluidic channel and then fixed and permeabilized to hybridize the fluorescence-labeled FISH probes to the complementary 16S rRNA sequences of the target microbes. D) Fluorescent imaging of magnetically captured bacteria ( E. coli : green, S. aureus : magenta).

Journal: medRxiv

Article Title: Quantitative fluorescence in situ hybridization (FISH) of magnetically confined bacteria enables rapid determination of early-stage human bacteremia

doi: 10.1101/2021.02.19.21251962

Figure Lengend Snippet: A schematic diagram of quantitative bacteremia identification using opsonin-coated MNPs and μFISH. A) Bacteria in bacteremia blood are magnetically captured and enriched by MNPs conjugated with human recombinant mannose-binding lectin (hrMBL-MNPs). B) The PDMS microfluidic device consists of eight inlets and outlets each for samples and FISH reagents, and 8 dividing channels for high throughput. C) Bacteria captured by the MNPs are magnetically confined in the microfluidic channel and then fixed and permeabilized to hybridize the fluorescence-labeled FISH probes to the complementary 16S rRNA sequences of the target microbes. D) Fluorescent imaging of magnetically captured bacteria ( E. coli : green, S. aureus : magenta).

Article Snippet: For targeting a wide range of bacteria, human recombinant mannose-binding lectin (hrMBL) (10405-HNAS, Sino Biological, China) was conjugated with MNPs in 200 nm size [ ] .

Techniques: Recombinant, Binding Assay, High Throughput Screening Assay, Fluorescence, Labeling, Imaging

The  MBL2  haplotype distribution among treatment naive patients with chronic HBV infection

Journal: Aging (Albany NY)

Article Title: Association study between mannose-binding lectin haplotypes and X gene mutation of hepatitis B virus from treatment naïve patients

doi: 10.18632/aging.101097

Figure Lengend Snippet: The MBL2 haplotype distribution among treatment naive patients with chronic HBV infection

Article Snippet: Human MBL2 quantikine ELISA kit (R&D systems, Minneapolis, MN, USA) was used to determine the serum level of MBL2.

Techniques:

The characteristics of treatment naive patients with chronic HBV infection

Journal: Aging (Albany NY)

Article Title: Association study between mannose-binding lectin haplotypes and X gene mutation of hepatitis B virus from treatment naïve patients

doi: 10.18632/aging.101097

Figure Lengend Snippet: The characteristics of treatment naive patients with chronic HBV infection

Article Snippet: Human MBL2 quantikine ELISA kit (R&D systems, Minneapolis, MN, USA) was used to determine the serum level of MBL2.

Techniques: Mutagenesis

The comparison of X gene mutation rate between groups divided by  MBL2  haplotypes

Journal: Aging (Albany NY)

Article Title: Association study between mannose-binding lectin haplotypes and X gene mutation of hepatitis B virus from treatment naïve patients

doi: 10.18632/aging.101097

Figure Lengend Snippet: The comparison of X gene mutation rate between groups divided by MBL2 haplotypes

Article Snippet: Human MBL2 quantikine ELISA kit (R&D systems, Minneapolis, MN, USA) was used to determine the serum level of MBL2.

Techniques: Comparison, Mutagenesis

The X gene mutation rate in high MBL2 group and medium/low MBL2 group.

Journal: Aging (Albany NY)

Article Title: Association study between mannose-binding lectin haplotypes and X gene mutation of hepatitis B virus from treatment naïve patients

doi: 10.18632/aging.101097

Figure Lengend Snippet: The X gene mutation rate in high MBL2 group and medium/low MBL2 group.

Article Snippet: Human MBL2 quantikine ELISA kit (R&D systems, Minneapolis, MN, USA) was used to determine the serum level of MBL2.

Techniques: Mutagenesis

The comparison of quasispecies complexity between groups divided by  MBL2  haplotypes

Journal: Aging (Albany NY)

Article Title: Association study between mannose-binding lectin haplotypes and X gene mutation of hepatitis B virus from treatment naïve patients

doi: 10.18632/aging.101097

Figure Lengend Snippet: The comparison of quasispecies complexity between groups divided by MBL2 haplotypes

Article Snippet: Human MBL2 quantikine ELISA kit (R&D systems, Minneapolis, MN, USA) was used to determine the serum level of MBL2.

Techniques: Comparison