rev: June 7, 2005
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CD CLUSTERED
ANTIBODIES
(anti-Human and others as indicated)
NOTE: . Please inquire for bulk or custom formulations (without preservative or carrier).
RDI div of Fitzgerald Industries Intl offers a wide line of antibodies. Since no one antibody works best for all applications (flow cytometry, neutralization, blotting, histochemistry, ELISA, etc), we offer many different types of antibodies to help solve this problem. Please inquire for other applications or types of antibodies not listed below. All products are for in vitro research use only-not for use in or on humans or animals-not for use in diagnostics. Price/availability/specifications subject to change without notice.
CD49b
Antibodies
Mouse anti-human CD49b antibodies
-2 clones & 1 polyclonal
CATALOG# CLONE# Workshop Host Form Price
RDI-M1540clb CLB-tromb/4, 10G11 IV mIgG1 purified $375.00
RDI-M1671clb " " " " FITC $375.00
RDI-CBL477 AK7 V mIgG1 purified $438.00
RDI-CBL477FT " " " " FITC $438.00
RDI-CBL477PE " " " " PE $531.00
RDI-CD49Babr rabbit poly
PeliCluster CD49e
cat#RDI-M1540clb
Test/vial 200
Clone CLB-tromb/4, 10G11
This clone has been derived from hybridization of SP2/0 cells with spleen
cells of a (BALB/c x A/J) mouse immunized with human T lymphocytes. This
antibody has been clustered to CD49b in the fifth international Workshop
on Human White Cell differentiation Antigens in Boston (1993).
Isotype Mouse IgG1.
Source Ascites fluid of tumour bearing BALB/c mice.
Purification Ammoniumsulphate precipitation and ion exchange chromatography.
Packing Each vial contains 1 ml with approximately 0.2 mg/ml monoclonal antibody
and 10 mg BSA in 20 mM TRIS and 150 mM NaCl, pH 8.0.
Preservative Mertiolate (0.001%). or sodium azide (see batch sheet)
Storage and stability Monoclonal antibodies should be stored in the dark
at 2-8°C. The reagent is stable until the expiry date stated on the
vial label.
Major reactivity The monoclonal antibody is directed against the CD49b- antigen
(GP Ia or VLA-2 alpha-chain), which can form distinct complexes with either
the CD29-antigen (GP IIa or VLA beta-chain), resulting in the VLA-2 (alpha-2
beta- 1) complex, which is expressed on human platelets. The monoclonal antibody
reacts with platelets, long-term cultivated T lymphocytes and activated T
lymphocytes. In immunohistology the monoclonal antibody reacts with thymocytes,
epithelial cells of a variety of tissues, peripheral nerves, fibroblasts,
osteoclasts, glomerular mesangium and most non-haemopoietic adherent cell
lines.
Molecular mass 130, 170 kDa.
Application Functional studies on cells.
Detection of human alloantibodies (anti-Bra,b) against VLA-2 (MAIPA assay).
Methods Indirect immunofluorescence staining with analysis by flowcytometry or fluorescence microscopy.
References
1. Knicki, T.J. et al., J. Biol. Chem., 263, 4516 (1988).
2. Giltay, J.C. et al., Blood, 73, 1235 (1989).
3. Staatz, W.D. et al., J. Cell. Biol. 108, 1917 (1989).
APPLICATION FOR AN INDIRECT IMMUNOFLUORESCENCE TECHNIQUE
Reagents
- FITC-conjugated goat anti-mouse immunoglobulin antiserum (M1204).
Remove aggregates by centrifugation at 1000 x g for 10 minutes.
- Buffer: Phosphate Buffered Saline (PBS), containing 0.2% Bovine Serum Albumin (BSA).
- PFA: Para-Formaldehyde 1%, pH 7.2, containing 0.2% BSA.
- Microtiter plates (96 wells, V bottom) or tubes.
Procedure
1 Fixate the cells with PFA 1% and wash them with buffer.
2 Prepare a mononuclear cell suspension with a concentration of 1 x 10 7 cells/ml in buffer.
3 Add 45 µl of cell suspension to the microtiter wells or tubes.
4 Add 5 µl monoclonal antibody to the microtiter wells or tubes and mix gently.
5 Incubate for 30 minutes at 2-8 C.
6 Add 100 µl buffer to the microtiter wells or 2 ml buffer to the tubes and centrifuge at 500 x g for 5 minutes.
7 Aspirate the supernatant from the cell pellet and resuspend the cells.
8 Add 200 µl buffer to the microtiter wells or 2 ml buffer to the tubes and centrifuge at 500 x g for 5 minutes.
9 Aspirate the supernatant from the cell pellet and resuspend the cells.
10 Add 50 µl FITC-conjugated goat anti-mouse immunoglobulin serum, solid phase adsorbed with human immunoglobulins, diluted 1:80.
11 Incubate for 30 minutes at 2-8 C.
12 Repeat step 6-9.
13 Add 200 µl buffer.
14 The number of positive cells can be determined by flowcytometry analysis or by means of fluorescence microscopy.
NOTE: Care should be taken when drawing blood to avoid activation of platelets.
Platelets activation markers are weakly expressed on platelets prepared from
directly fixed normal whole blood.
The expression is maximal on thrombin (1 U/ml) stimulated washed platelets.
FOR IN VITRO RESEARCH USE ONLY
PeliCluster CD49b F
cat#RDI-M1671clb
Test/vial 100
Clone CLB-tromb/4, 10G11
This clone has been derived from hybridization of SP2/0 cells with spleen
cells of a (BALB/c x A/J) mouse immunized with human T lymphocytes. This
antibody has been clustered to CD49b in the fifth international Workshop
on Human White Cell differentiation Antigens in Boston (1993).
Isotype Mouse IgG1.
Source Ascites fluid of tumour bearing BALB/c mice.
Purification Ammoniumsulphate precipitation and ion exchange chromatography.
Conjugation Cojugated with fluorescein iso thiocyanate isomer 1 (FITC).
Molecular F/P ratio between 6.0 - 10.0
Packing Each vial contains 1 ml FITC conjugated monoclonal antibody and 10
mg BSA in PBS.
Preservative Mertiolate (0.001%) or sodium azide
Storage and stability Monoclonal antibodies should be stored in the dark
at 2-8°C. The reagent is stable until the expiry date stated on the
vial label.
Major reactivity The monoclonal antibody is directed against the CD49b- antigen
(GP Ia or VLA-2 alpha-chain), which can form distinct complexes with either
the CD29-antigen (GP IIa or VLA beta-chain), resulting in the VLA-2 (alpha-2
beta- 1) complex, which is expressed on human platelets. The monoclonal antibody
reacts with platelets, long-term cultivated T lymphocytes and activated T
lymphocytes. In immunohistology the monoclonal antibody reacts with thymocytes,
epithelial cells of a variety of tissues, peripheral nerves, fibroblasts,
osteoclasts, glomerular mesangium and most non-haemopoietic adherent cell
lines.
Molecular mass 130, 170 kDa.
Application Detection of human alloantibodies (anti-Bra,b) against VLA-2
(MAIPA assay).
Methods Direct immunofluorescence staining with analysis by flowcytometry
or fluorescence microscopy.
References
1. Knicki, T.J. et al., J. Biol. Chem., 263, 4516 (1988).
2. Giltay, J.C. et al., Blood, 73, 1235 (1989).
3. Staatz, W.D. et al., J. Cell. Biol. 108, 1917 (1989).
FOR IN VITRO RESEARCH USE ONLY
PRODUCT CODE :RDI-CBL477 $438.00/vial 200ug
Also available FITC labeled cat#RDI-CBL477-FT $438.00/100 tests
PE labeled cat#RDI-CBL477-PE $531.00/100 tests
CLONE: AK7
ISOTYPE: IgG1
SOURCE: Mouse ascitic fluid
PURIFICATION METHOD: Ammonium sulphate precipitation folloed by ion exchange
chromatography.
SPECIFICITY: Human platelet antigen (Mr 170kD). The antigen is found on
platelets, endothelial cells and approximately 50% of monocytes together
with activated T cells. The gpla antigen is non- covalently associated with
the 130kD VLA ß-chain (CD29) in the VLA-2 complex.
APPLICATIONS:
*This antibody reacts with the platelet gp Ia molecule (a-chain of the adhesion molecule VLA-2), the platelet collagen receptor.
* Detection of human alloantibodies against VLA-2.
REFERENCES:
Favaloro, E.J. et al. Bs. J. Haem. 74, 385 - 94 (1990)
Mazurov, A.V. et al. Thromb. Haemost. 66, 494 - 99 (1991)
PRESENTATION: Each monoclonal is delivered in a sealed vial at a concentration of 2 vial of 100ug/1ml each in phosphate buffered saline solution containing 10mM sodium azide and 1mg/ml BSA. We recommend that each laboratory determine an optimum working titre for use in its particular application.
STORAGE: Purified monoclonal antibodies are generally stable for long periods
at 4oC. However repeated warming to room temperature and re-cooling may result
in a loss of activity and hence effective working titre. It is recommended
that monoclonal antibodies are aliquotted upon receipt and then stored at
-20C. After thawing they should then be used as a stock solution for up to
60 days. Dilute working solutions are best prepared on the day of use.
For research use only. Not supplied for use in human diagnostic or therapeutic
procedures
Catalog#: RDI-CD49Babr $469.00
Package Size: 100ul ,liquid neat sera with 0.05% sodium azide
Species: rabbit polyclonal
Immunogen: synthetic peptide derived from the c terminal cytoplasmic domain of human alpha2 integrin subunit
(KYEKMTKNPDEODETTELSS)
Reactivity: reacts with CD49B (alpha 2 integrin subunit in human. Sees a cytoplasmic/intracellular epitope. No cross observed with alpha-1, alpha-3, alpha4, alpha5, alpha6 or alpha V subunits
species: Human, rat, mouse, hamster, chicken
Uses: -immunoblotting(non reducing conditions may be better) 1:1000
-immunoprecipitation: 5ul per 5 million cells
-acetone fixed frozen tissue
Titers must be optimized for each application
ref: Deroanne, CF et al, Exper Cell Res (1996) 224:215-223
Storage: Store at -20 DEG C in undiluted aliquots. For extensive dilutions, add protein containing or stabilizing medium. Avoid frequent freeze thaw cycles.
Precautions: For In vitro research Use Only. No for use in or on humans or animals or for diagnostics.
Note: Upon receipt, tighten cap, and centrifuge for 1-2 minutes at 1000 RPM to concentrate antibody in vial (during shipping, some antibody can become lodged inside the cap and on sides of vial
34 Junction Square Drive
Concord MA 01742-3049 USA
phone (978) 371-6446
fax (978) 371-2266
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