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APC anti-human CD14 Antibody

Pricing & Availability
Clone
HCD14 (See other available formats)
Regulatory Status
RUO
Other Names
LPS receptor
Isotype
Mouse IgG1, κ
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Product Citations
publications
HCD14_APC_061407
Human peripheral blood monocytes stained with HCD14 APC
  • HCD14_APC_061407
    Human peripheral blood monocytes stained with HCD14 APC
Compare all formats See APC spectral data
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325607 25 tests 110€
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325608 100 tests 233€
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Description

CD14 is a 53-55 kD glycosylphosphatidylinositol (GPI)-linked membrane glycoprotein also known as LPS receptor. CD14 is expressed at high levels on monocytes and macrophages, and at lower levels on granulocytes. Some dendritic cell populations such as interfollicular dendritic cells, reticular dendritic cells, and Langerhans cells have also been reported to express CD14. As a high-affinity receptor for LPS, CD14 is involved in the clearance of gram-negative pathogens and in the upregulation of adhesion molecules and cytokines expression in monocytes and neutrophils.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Human
Antibody Type
Monoclonal
Host Species
Mouse
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and BSA (origin USA)
Preparation
The antibody was purified by affinity chromatography, and conjugated with APC under optimal conditions.
Concentration
Lot-specific (to obtain lot-specific concentration and expiration, please enter the lot number in our Certificate of Analysis online tool.)
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Application

FC - Quality tested
Recommended Usage

Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For flow cytometric staining, the suggested use of this reagent is 5 µl per million cells in 100 µl staining volume or 5 µl per 100 µl of whole blood.

Excitation Laser
Red Laser (633 nm)
Application Notes

Additional reported applications (for the relevant formats) include: immunofluorescence microscopy. This clone was tested in-house and does not work on formalin fixed paraffin-embedded (FFPE) tissue.

Application References
  1. McMichael A, et al. 1987. Leucocyte Typing III. Oxford University Press. New York.
  2. Knapp W, et al. Eds. 1989. Leucocyte Typing IV. Oxford University Press. New York.
  3. Schlossman S, et al. Eds. 1995. Leucocyte Typing V. Oxford University Press. New York.
Product Citations
  1. Colonna L, et al. 2016. Clin Immunol. 163:84-90. PubMed
  2. Guo X, et al. 2016. Mol Ther Methods Clin Dev. 3:15054. PubMed
  3. Xun X, et al. 2021. Am J Transl Res. 13:4360. PubMed
  4. Lamichhane R, et al. 2020. Eur J Immunol. 50:178. PubMed
  5. Hearnden R, et al. 2021. STAR Protocols. 2(2):100422. PubMed
  6. Allegrezza M, et al. 2016. Cancer Res . 76: 6253 - 6265. PubMed
  7. Wang E, et al. 2021. Cell Stem Cell. 28(4):718-731.e6. PubMed
  8. Zhong J, et al. 2018. Sci Adv. 4:eaas9864. PubMed
  9. Liu Y, et al. 2021. Front Immunol. 11:579372. PubMed
  10. Schepp J, et al. 2017. Arthritis Rheumatol. 69:1689. PubMed
  11. Wang Y, et al. 2021. Sci Rep. 1.429861111. PubMed
  12. Keller M, et al. 2013. PLoS One. 12:79601. PubMed
  13. Pellegrini JM, et al. 2021. Sci Rep. 11:13559. PubMed
  14. Collins D, et al. 2015. PLoS Pathog. 11: 1005054. PubMed
  15. Fisch D, et al. 2022. Pathog Dis. 79:. PubMed
  16. Fu W, et al. 2016. Sci Rep. 6:38162. PubMed
  17. Rohner L, et al. 2020. Sci Rep. 0.570833333. PubMed
  18. Hakimi AA, et al. 2019. Cancer Discov. 9:510. PubMed
  19. Zhu Y, et al. 2019. Cell Stem Cell. 25:542. PubMed
  20. Vabret N, et al. 2022. iScience. 25:104599. PubMed
  21. Li YR, et al. 2021. Cell Rep Med. 2:100449. PubMed
  22. Akoumianaki T, et al. 2021. Cell Host Microbe. . PubMed
  23. Fujisaka Y, et al. 2018. Oncol Lett. 15:509. PubMed
  24. Molina MS, et al. 2021. Front Immunol. 12:699128. PubMed
  25. Domanska D, et al. 2022. J Exp Med. 219:. PubMed
  26. Wee Y, et al. 2016. Exp Biol Med. 241: 1217 - 1228. PubMed
  27. Cointe S, et al. 2018. J Extracell Vesicles. 7:1494482. PubMed
RRID
AB_830680 (BioLegend Cat. No. 325607)
AB_830681 (BioLegend Cat. No. 325608)

Antigen Details

Structure
GPI-linked membrane glycoprotein, 53-55 kD
Distribution

Monocytes, macrophages, granulocytes (low)

Function
LPS receptor, clearance of Gram-negative pathogens
Ligand/Receptor
LPS
Cell Type
Granulocytes, Macrophages, Monocytes, Neutrophils
Biology Area
Cell Biology, Immunology, Innate Immunity, Neuroinflammation, Neuroscience
Molecular Family
CD Molecules
Antigen References

1. Stocks S, et al. 1990. Biochem. J. 268:275.
2. Wright S, et al. 1990. Science 249:1434.

Gene ID
929 View all products for this Gene ID
UniProt
View information about CD14 on UniProt.org

Related FAQs

There are no FAQs for this product.
Go To Top Version: 2    Revision Date: 07-13-2015

For research use only. Not for diagnostic use. Not for resale. BioLegend will not be held responsible for patent infringement or other violations that may occur with the use of our products.

 

*These products may be covered by one or more Limited Use Label Licenses (see the BioLegend Catalog or our website, www.biolegend.com/ordering#license). BioLegend products may not be transferred to third parties, resold, modified for resale, or used to manufacture commercial products, reverse engineer functionally similar materials, or to provide a service to third parties without written approval of BioLegend. By use of these products you accept the terms and conditions of all applicable Limited Use Label Licenses. Unless otherwise indicated, these products are for research use only and are not intended for human or animal diagnostic, therapeutic or commercial use.

 

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This data display is provided for general comparisons between formats.
Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
If you need assistance with selecting the best format contact our expert technical support team.

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