Mouse monoclonal [MLR2] to p75 NGF Receptor (FITC)
ConjugationFITC. Ex: 493nm, Em: 528nm
Conjugation notesThe antibody was conjugated to Fluorescein isomer 1 (FITC, Sigma). A minimum fluorescein: protein ratio of 3:1 is guaranteed. The conjugate was purified via gel filtration using a G25 fine grain gel in 10 mMTris/50mM NaCl solution.
SpecificityReacts with human, mouse and rat. Other species have not yet been tested but it is expected that this antibody will be useful for the study of p75 in primates and other species.
Purification notesImmunoglobulin (IgG2A) was purified using Protein G column (Amersham Pharmacia), polished with Sephacryl 200HR (Amersham Pharmacia) in PBS and then lyophilized. Purity was analysed using electrophoresis, 4-12% Bis Tris Gel (Invitrogen).
Clonality Monoclonal
Clone numberMLR2
IsotypeIgG2a
Research Areas
Neuroscience
Neurology process
Growth and Development
Neurotrophins
Stem Cells
Neural Stem Cells
Surface Molecules
Stem Cells
Mesenchymal Stem Cells
Surface Molecules
Applications
Our Abpromise guarantee covers the use of ab62122 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Application
Notes
ICC/IF
ICC/IF: Use a concentration of 1 - 2 µg/ml.
Flow Cyt
Flow Cyt: 1/10. (paraformaldehyde or methanol fixed cells)
ELISA
ELISA: 1/5000.
Application notesIs unsuitable for ,BL or WB.
Target
FunctionLow affinity receptor which can bind to NGF, BDNF, NT-3, and NT-4. Can mediate cell survival as well as cell death of neural cells.
Sequence similaritiesContains 1 death domain. Contains 4 TNFR-Cys repeats.
DomainDeath domain is responsible for interaction with RANBP9. The extracellular domain is responsible for interaction with NTRK1.
Post-translational modificationsN- and O-glycosylated. O-linked glycans consist of Gal(1-3)GalNAc core elongated by 1 or 2 NeuNAc. Phosphorylated on serine residues.
Overlay histogram showing PC12 cells stained with ab62122 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab62122, 1/10 dilution) for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 2µg/1x106 cells) with secondary antibody DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Acquisition of >5,000 events was performed. This antibody gave a positive signal in PC12 cells fixed with methanol (5 min) used under the same conditions.
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