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FITC anti-human CD271 (NGFR) Antibody

Pricing & Availability
Clone
ME20.4 (See other available formats)
Regulatory Status
RUO
Other Names
p75NTR, TNFRSF16, p75(NTR), Gp80-LNGFR, NGFR, Nerve Growth Factor Receptor
Isotype
Mouse IgG1, κ
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Product Citations
publications
ME20.4_FITC_110309
Human neuroblastoma cell line SK-N-MC stained with ME20.4 FITC
  • ME20.4_FITC_110309
    Human neuroblastoma cell line SK-N-MC stained with ME20.4 FITC
See FITC spectral data
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345103 25 tests 104€
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345104 100 tests 207€
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Description

CD271, also known as p75NTR, TNFRSF16, p75(NTR), Gp80-LNGFR, and NGFR, is a type I transmembrane protein with a MW of 75 kD. It is expressed by many cell types including neurons, Schwann cells, mesenchymal stem/stromal cells, follicular dendritic cells and melanocytes. The extracellular portion contains four TNFR-Cys repeats that form the binding domain for its ligands (NGF, BDNF, NTF3, and NTF4). The intracellular portion of CD271 contains a death domain, which interacts with TRAF2, TRAF4, TRAF6, PTPN13 and RANBP9, to promote cell apoptosis, and to regulate cell differentiation and neurogenesis.

Product Details
Technical Data Sheet (pdf)

Product Details

Reactivity
Human
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
WM245 melanoma cells
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 FITC 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
Blue Laser (488 nm)
Application Notes

Additional reported applications for the relevant formats include: immunoprecipitation1, Western blotting4, immunohistochemical staining of frozen or paraffin embedded tissue sections1,2, and blocking of NGF binding1.

Application References
  1. Ross A, et al. 1984. P. Natl. Acad. Sci. USA 81:6681. (FC, IP, Block, IHC)
  2. Cattoretti G, et al. 1993. Blood 81:1726. (IHC)
  3. Kamke MR, et al. 2005. Hear Res. 206:89.
  4. Baker D, et al. 1989. Cancer Res. 49:4142-4146. (FC, WB)
Product Citations
  1. Kagoya Y, et al. 2018. Nat Commun. 9:1915. PubMed
  2. Lin JR et al. 2018. eLife. 7 pii: e31657. PubMed
  3. Dige A, et al. 2019. Gastroenterology. 156:2208. PubMed
  4. Naamati A, et al. 2019. Elife. 8:e41431. PubMed
  5. Kowal JM, et al. 2019. Stem Cells Transl Med. 0.50625. PubMed
  6. Liu W, et al. 2020. Int J Biol Sci. 0.725694444. PubMed
  7. Yoshida H, et al. 2020. Sci Rep. 1.249305556. PubMed
  8. Zuo J, et al. 2013. J Virol. 87:5340. PubMed
  9. Aomatsu E, et al. 2014. Sci Rep. 4:3652. PubMed
  10. Nakatsugawa M, et al. 2015. J Immunol. 194 3487 . PubMed
  11. Ochi T, et al. 2015. Cancer Immunol Res. 3: 1070-1081. PubMed
  12. Nakatsugawa M, et al. 2016. Sci Rep. 6:23821. PubMed
  13. Yang R, et al. 2020. Cell. 183(7):1826-1847.e31. PubMed
  14. Kenswil KJG, et al. 2021. Cell Stem Cell. 28(4):653-670.e11. PubMed
  15. Yamamoto K, et al. 2021. Cell Reports. 36(8):109576. PubMed
  16. Marelli S, et al. 2020. Elife. :9. PubMed
  17. Bonny AR, et al. 2021. Nat Commun. 12:292. PubMed
  18. Kowal JM, et al. 2021. Stem Cell Res Ther. 12:265. PubMed
  19. Liu S, et al. 2021. Mol Ther. 29:1918. PubMed
  20. Tencerova M, et al. 2021. Stem Cell Res Ther. 12:586. PubMed
  21. Murata K, et al. 2020. Elife. 9:. PubMed
  22. Jann JC, et al. 2021. Nat Commun. 12:6170. PubMed
  23. Shalabi SF, et al. 2021. Nat Aging. 1:838. PubMed
  24. Jia L, et al. 2022. Ann Transl Med. 10:482. PubMed
  25. Guo D, et al. 2022. Elife. 11:. PubMed
  26. Li L, et al. 2020. J Transl Med. 18:363. PubMed
  27. Rodrigues Toste de Carvalho AL, et al. 2021. Nat Protoc. 16:1802. PubMed
  28. Guo D, et al. 2022. Bio Protoc. 12:. PubMed
  29. Lumaquin D, et al. 2023. Nat Commun. 14:3192. PubMed
RRID
AB_1937226 (BioLegend Cat. No. 345103)
AB_2282828 (BioLegend Cat. No. 345104)

Antigen Details

Structure
Type I transmembranal protein with a MW of 75 kD. The extracellular portion contains four TNFR-Cys repeats that form the NGF binding domain; the intracellular portion contains a death domain.
Distribution

Expressed by many cell types including neurons, Schwann cells, mesenchymal stem/stromal cells, follicular dendritic cells, melanocytes.

Function
Apoptosis, differentiation, neurogenesis.
Interaction
TRAF2, TRAF4, TRAF6, PTPN13, RANBP9.
Ligand/Receptor
Nerve growth factor (NGF), Brain-derived neurotrophic factor (BDNF), Neurotrophin 3. (NTF3) , Neurotrophin 4 (NTF4)
Bioactivity
Apoptosis, differentiation, neurogenesis.
Cell Type
Dendritic cells, Mesenchymal cells, Mesenchymal Stem Cells, Neurons
Biology Area
Apoptosis/Tumor Suppressors/Cell Death, Cell Biology, Immunology, Neuroscience, Stem Cells, Synaptic Biology
Molecular Family
CD Molecules, Cytokine/Chemokine Receptors, Postsynaptic proteins
Antigen References

1. Friedman MJ, et al. 2009. J. Biol. Chem. 284:27944.
2. Rock JR, et al. 2009. Proc Natl Acad Sci USA. 106:12771.
3. Kidd SK, et al. 2008. Brain Res.1195:113.
4. Peters EM, et al. 2007. Am J Pathol. 171:1872.
5. Jansen P, et al. 2007. Nat Neurosci. 10:1449.

Gene ID
4804 View all products for this Gene ID
UniProt
View information about CD271 on UniProt.org

Related FAQs

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Go To Top Version: 1    Revision Date: 11/30/2012

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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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