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pattern-recognition molecule  (MBL Life science)

 
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    Structured Review

    MBL Life science pattern-recognition molecule
    Pattern Recognition Molecule, supplied by MBL Life science, 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/pattern-recognition+molecule/pattern+recognition+molecules/pm25579818-1-5-29
    Average 90 stars, based on 1 article reviews
    pattern-recognition molecule - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Binding Assay:

    Article Title: Complement and fungal pathogens: an update.
    Article Snippet: Fungal infections are a serious complication in immunocompromised patients such as human immunodeficiency virus-infected individuals, patients with organ transplantations or with haematological neoplasia.. The lethality of opportunistic fungal infection is high despite a growing arsenal of antimycotic drugs, implying the urgent need for supportive immunological therapies to strengthen the current inefficient antimicrobial defences of the immunocompromised host.. Therefore, increasing effort has been directed to investigating the interplay between fungi and the host immunity and thus to find starting points for additional therapeutic approaches.

    Incubation:

    Article Title: Complement and fungal pathogens: an update.
    Article Snippet: Fungal infections are a serious complication in immunocompromised patients such as human immunodeficiency virus-infected individuals, patients with organ transplantations or with haematological neoplasia.. The lethality of opportunistic fungal infection is high despite a growing arsenal of antimycotic drugs, implying the urgent need for supportive immunological therapies to strengthen the current inefficient antimicrobial defences of the immunocompromised host.. Therefore, increasing effort has been directed to investigating the interplay between fungi and the host immunity and thus to find starting points for additional therapeutic approaches.

    Activation Assay:

    Article Title: Complement and fungal pathogens: an update.
    Article Snippet: Fungal infections are a serious complication in immunocompromised patients such as human immunodeficiency virus-infected individuals, patients with organ transplantations or with haematological neoplasia.. The lethality of opportunistic fungal infection is high despite a growing arsenal of antimycotic drugs, implying the urgent need for supportive immunological therapies to strengthen the current inefficient antimicrobial defences of the immunocompromised host.. Therefore, increasing effort has been directed to investigating the interplay between fungi and the host immunity and thus to find starting points for additional therapeutic approaches.

    other:

    Article Title: Structural insights into the initiating complex of the lectin pathway of complement activation.
    Article Snippet: d The architecture of a pattern-recognition molecule bound to an MASP protease revealed d A remarkably large nonglobular structure visualized by SAXS and electron microscopy d MASP-1 protrudes from MBL, separating the SP domains by more than 200 Å in solution d Our structural studies support an intercomplexmode of lectin pathway activation Kjaer et al., 2015, Structure 23, 342–351 February 3, 2015 a2015 Elsevier Ltd All rights reserved http://dx.doi.org/10.1016/j.str.2014.10.024 Authors

    Article Title: The complement system in glioblastoma multiforme
    Article Snippet: After breaching the host’s environmental barriers, invading microbes are detected by the pattern recognition molecules (PRM) of the classical (C1q) and lectin (MBL, ficolins) complement pathways (CP, LP) [ , ]. (Fig. ).



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    MASPs and MAp44 levels in T1D patients stratified by IR status. A: MASP-1; B: MASP-2; C: MASP-3; D: MAp44. *Significant association at P < 0.05; **a significant association at P < 0.001; ***a significant association at P < 0.0001; closed circles = eGDR < 5.1, gray circles = eGDR 5.1–8.7; open circles = eGDR > 8.7; MASP = mannan-binding <t>lectin-associated</t> <t>serine</t> <t>proteases;</t> MAp44 = mannose-binding lectin-associated protein.
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    MASPs and MAp44 levels in T1D patients stratified by IR status. A: MASP-1; B: MASP-2; C: MASP-3; D: MAp44. *Significant association at P < 0.05; **a significant association at P < 0.001; ***a significant association at P < 0.0001; closed circles = eGDR < 5.1, gray circles = eGDR 5.1–8.7; open circles = eGDR > 8.7; MASP = mannan-binding <t>lectin-associated</t> <t>serine</t> <t>proteases;</t> MAp44 = mannose-binding lectin-associated protein.
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    Image Search Results


    MASPs and MAp44 levels in T1D patients stratified by IR status. A: MASP-1; B: MASP-2; C: MASP-3; D: MAp44. *Significant association at P < 0.05; **a significant association at P < 0.001; ***a significant association at P < 0.0001; closed circles = eGDR < 5.1, gray circles = eGDR 5.1–8.7; open circles = eGDR > 8.7; MASP = mannan-binding lectin-associated serine proteases; MAp44 = mannose-binding lectin-associated protein.

    Journal: Clinical and Experimental Immunology

    Article Title: Plasma levels of mannan-binding lectin-associated serine proteases are increased in type 1 diabetes patients with insulin resistance

    doi: 10.1093/cei/uxad113

    Figure Lengend Snippet: MASPs and MAp44 levels in T1D patients stratified by IR status. A: MASP-1; B: MASP-2; C: MASP-3; D: MAp44. *Significant association at P < 0.05; **a significant association at P < 0.001; ***a significant association at P < 0.0001; closed circles = eGDR < 5.1, gray circles = eGDR 5.1–8.7; open circles = eGDR > 8.7; MASP = mannan-binding lectin-associated serine proteases; MAp44 = mannose-binding lectin-associated protein.

    Article Snippet: Activation of the lectin pathway is mediated by mannan-binding lectin (MBL) pattern recognition molecules via MBL-associated serine proteases (MASPs) and regulatory MBL-associated proteins (MAps), although the role and action of some of these components are yet to be fully elucidated [ ].

    Techniques: Binding Assay