R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
FcRn (E4D5I) Rabbit mAb #20085
Filter:
- WB
- IHC
Supporting Data
| REACTIVITY | M R |
| SENSITIVITY | Endogenous |
| MW (kDa) | 50-60 |
| Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IHC-Immunohistochemistry
Species Cross-Reactivity Key:
- M-Mouse
- R-Rat
Product Information
Product Usage Information
| Application | Dilution |
|---|---|
| Western Blotting | 1:1000 |
| Immunohistochemistry (Paraffin) | 1:50 - 1:200 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
FcRn (E4D5I) Rabbit mAb recognizes endogenous levels of total FcRn protein. Non-specific staining was observed in mouse stomach by immunohistochemistry.
Species Reactivity:
Mouse, Rat
Source / Purification
Monoclonal antibody is produced by immunizing animals with mouse FcRn recombinant protein.
Background
The neonatal Fc receptor, FcRn, is an atypical Fc gamma receptor that bears homology to class I MHC (major histocompatibility complex) and associates with β2-microglobulin (1). FcRn is expressed by the vascular endothelium, several epithelial cell types, and hematopoietic cells including several innate immune cell types and B cells (2). FcRn mediates recycling and transcytosis of IgG, resulting in protection of IgG from catabolism and an extended serum half-life of IgG relative to other antibody isotypes (3). In addition, FcRn transports IgG across the placenta and also mediates uptake of maternal IgG from milk, resulting in enhanced humoral immunity in the fetus and neonates (1,4,5). FcRn also plays an important role in initiation of adaptive immunity by transporting immune complexes to intracellular dendritic cell compartments for antigen processing and presentation to T cells (6-8). In addition to IgG, FcRn also binds albumin and similarly protects it from catabolism, leading to extended half-life and high plasma concentrations (9).
- Simister, N.E. and Mostov, K.E. (1989) Nature 337, 184-7.
- Pyzik, M. et al. (2015) J Immunol 194, 4595-603.
- Roopenian, D.C. et al. (2003) J Immunol 170, 3528-33.
- Story, C.M. et al. (1994) J Exp Med 180, 2377-81.
- Raghavan, M. et al. (1994) Immunity 1, 303-15.
- Yoshida, M. et al. (2006) Springer Semin Immunopathol 28, 397-403.
- Qiao, S.W. et al. (2008) Proc Natl Acad Sci U S A 105, 9337-42.
- Baker, K. et al. (2011) Proc Natl Acad Sci U S A 108, 9927-32.
- Chaudhury, C. et al. (2003) J Exp Med 197, 315-22.
限制使用
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