C3ar1 Mouse Monoclonal Antibody [Clone ID: 74]

CAT#: AM31834FC-N

C3ar1 mouse monoclonal antibody, clone 74, FITC


USD 290.00

2 Weeks*

Size
    • 100 ug

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Specifications

Product Data
Clone Name 74
Applications FC, IHC
Recommended Dilution Flow Cytometry.
Immunohistochemistry on frozen sections.
Reactivities Rat
Host Mouse
Isotype IgG1
Clonality Monoclonal
Immunogen RBL-2H3 transfectants expressing rat C3aR
Donor: BALB/c
Fusion Partner: X63-Ag8.653
Specificity This rat C3a receptor antibody detects a recombinant peptide corresponding to amino acids 161-321 of the large extracellular loop structure, which shares 34% homology with mouse and human. Deduced amino acid sequences of human/rat C3aR is 58.5% and 90.7% with rat/mouse.
Formulation PBS containing 0.02% sodium azide (NaN3) as preservative and EIA grade BSA was added as a stabilizing protein to bring the total protein concentration to 4-5 mg/ml.
Label: FITC
State: Liquid purified Ig fraction
Label: Fluorescein isothiocyanate isomer 1
Concentration 0,1 mg/ml
Purification Affinity chromatography on Protein G
Conjugation FITC
Gene Name Rattus norvegicus complement C3a receptor 1 (C3ar1)
Background C3aR binds to anaphylotoxin C3a which, among other things, is involved in mast cell degranulation and recruitment of immune cells to the site of inflammation. Activation of the complement cascade produces various fragments, including C3a and C5a.
C3aR is characterized by seven transmembrane domains including a large extracellular loop which is coupled to a Gi protein. C3aR expression is detected on glial cells, neurons and cells belonging to the mononuclear phagocyte system. C3aR expression was shown to moderately increase after LPS stimulation.
Synonyms C3a-R, C3AR, C3AR1, AZ3B, C3R1, HNFAG09
Note Protocol: FLOW CYTOMETRY ANALYSIS:
Method:
1. Prepare a cell suspension in media A. For cell preparations, deplete the red blood cell population with Lympholyte®-Rat cell separation medium.
2. Wash 2 times.
3. Resuspend the cells to a concentration 2x10e7 cells/ml in media A. Add 50 μl of this suspension to each tube (each tube will then contain 1x10e6 cells, representing 1 test).
4. To each tube, add 0.5μg of this antibody.
5. Vortex the tubes to ensure thorough mixing of antibody and cells.
6. Incubate the tubes for 30 minutes at 4°C.
7. Wash 2 times at 4°C.
8. Add 100 μl of secondary antibody (FITC Goat anti-mouse IgG) at 1/500 dilution.
9. Incubate the tubes at 4°C for 30-60 minutes.
(It is recommended that the tubes are protected from light since most fluorochromes are light sensitive).
10. Wash 2 times at 4°C in media B.
11. Resuspend the cell pellet in 50 μl ice cold media B.
12. Transfer to suitable tubes for flow cytometric analysis containing 15 μl of propidium iodide at 0.5 mg/ml in PBS. This stains dead cells by intercalating in DNA.

Media:
A. Phosphate buffered saline (pH 7.2) + 5% normal serum of host species + sodium azide (100 μl of 2M sodium azide in 100 mls).
B. Phosphate buffered saline (pH 7.2) + 0.5% Bovine serum albumin + sodium azide (100 μl of 2M sodium azide in 100 mls).

Results:
Tissue Distribution by Flow Cytometry Analysis:
Rat Strain: Wistar
Cell Concentration: 1x10e6 cells per test
Antibody Concentration Used: 2.0μg /106 cells
Isotypic Control: FITC Mouse IgG1
Cell Source:
Peritoneal Macrophages 97.2%
Bone Marrow 81.5%
Reference Data

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