Human MBL2 ELISA Kit (V2LY-0626-LY4129)

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Tested Data
Request for COA
Datasheet Target References Q & As Review & reward Protocols Associated Products

Basic Information

Sensitivity
2.41 ng/mL
Detection Range
5-1000 ng/mL
Sample Type
Serum, Plasma, cell culture supernates
Specificity
Human
Assay Type
Sandwich
Reactivity
Human
Assay Time
1.5 h
Molecule Mass
26.1 kDa
Components
  • Pre-coated ELISA Plate: 12 wells * 8 detachable strips
  • Standard solution: 0.5ml x1
  • Standard diluent: 3ml x1
  • Streptavidin-HRP: 6ml x1
  • Stop solution: 6ml x1
  • Substrate solution A: 6ml x1
  • Substrate solution B: 6ml x1
  • Wash buffer concentrate (25x): 20ml x1
  • Biotinylated antibody: 1ml x1

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at 2-8°C
More Infomation

Target

Full Name
Mannose Binding Lectin 2
Function
Calcium-dependent lectin involved in innate immune defense (PubMed:35102342).

Binds mannose, fucose and N-acetylglucosamine on different microorganisms and activates the lectin complement pathway. Binds to late apoptotic cells, as well as to apoptotic blebs and to necrotic cells, but not to early apoptotic cells, facilitating their uptake by macrophages. May bind DNA. Upon SARS coronavirus-2/SARS-CoV-2 infection, activates the complement lectin pathway which leads to the inhibition SARS-CoV-2 infection and a reduction of the induced inflammatory response (PubMed:35102342).
Biological Process
Acute-phase response Source: BHF-UCL
Cell surface pattern recognition receptor signaling pathway Source: ComplexPortal
Complement activation, classical pathway Source: UniProtKB-KW
Complement activation, lectin pathway Source: MGI
Defense response to bacterium Source: BHF-UCL
Defense response to Gram-positive bacterium Source: MGI
Innate immune response Source: BHF-UCL
Killing by host of symbiont cells Source: Ensembl
Negative regulation of viral process Source: BHF-UCL
Opsonization Source: BHF-UCL
Positive regulation of opsonization Source: ComplexPortal
Proteolysis Source: ComplexPortal
Response to oxidative stress Source: UniProtKB
Cellular Location
Secreted

Liao, H., Yang, J., Xu, Y., Xie, J., Li, K., Chen, K., ... & Pan, M. (2023). Mannose-Binding Lectin 2 as a Potential Therapeutic Target for Hepatocellular Carcinoma: Multi-Omics Analysis and Experimental Validation. Cancers, 15(19), 4900.

Uysalol, M., Gumus, S., Yildiz, R., Pasli Uysalol, E., Pehlivan, S., Pehlivan, M., & Serin, I. (2022). Importance of mannose-binding lectin2 polymorphism (rs1800450) in infections in children. Biomarkers, 27(1), 44-49.

Doulami, C., Kishore, U., Sim, R. B., & Schwaeble, W. (2021). Mannose-binding lectin in human health and disease. The Collectin Protein Family and Its Multiple Biological Activities, 17-47.

Kalia, N., Singh, J., & Kaur, M. (2021). The ambiguous role of mannose-binding lectin (MBL) in human immunity. Open Medicine, 16(1), 299-310.

Bąk-Romaniszyn, L., Świerzko, A. S., Sokołowska, A., Durko, Ł., Mierzwa, G., Szala-Poździej, A., ... & Cedzyński, M. (2020). Mannose-binding lectin (MBL) in adult patients with inflammatory bowel disease. Immunobiology, 225(1), 151859.

Polesello, V., Segat, L., Biasotto, M., Ottaviani, G., Gobbo, M., Di Lenarda, R., ... & Zupin, L. (2019). Mannose-Binding Lectin 2 (MBL2) combined genotypes deficiency is associated with susceptibility for Oral Lichen Planus. Genetics and Molecular Biology, 42, 9-14.

Tong, X., Wan, Q., Li, Z., Liu, S., Huang, J., Wu, M., & Fan, H. (2019). Association between the mannose-binding lectin (MBL)-2 gene variants and serum MBL with pulmonary tuberculosis: An update meta-analysis and systematic review. Microbial pathogenesis, 132, 374-380.

Ulrich-Merzenich, G., Hausen, A., Zeitler, H., Goldmann, G., Oldenburg, J., & Pavlova, A. (2019). The role of variant alleles of the mannose-binding lectin in the inhibitor development in severe hemophilia A. Thrombosis Research, 179, 140-146.

Videbaek, K., Buchvald, F., Holgersen, M. G., Henriksen, A., Eriksson, F., Garred, P., & Nielsen, K. G. (2019). The impact of mannose‐binding lectin polymorphisms on lung function in primary ciliary dyskinesia. Pediatric Pulmonology, 54(8), 1182-1189.

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For research use only. Not intended for any clinical use.

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