lambda antibody (CF405M)

Catalog No. ABIN1112415

Product Details

Target: lambda

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: CF405M

Application: Flow Cytometry (FACS), Immunofluorescence (IF)

Characteristics: Mouse Monoclonal Anti-Human Lambda CFTMBlue is recommended for use in flow cytometry for identification of Lamba immunoglobulin light chain, to study the presence and extent of clonal expansion in B-lymphoproliferative disorders. Abnormal kappa/lambda ratios or intensities are strong indicators of clonal processes.The conjugate is provided in liquid form in buffer containing an antibody stabilizer solution and 0,09% NaN3, pH 7.2.

Clone: HIglambda

Isotype: IgG3

Application Details

Application Notes: It is recommended for use in flow cytometry. This reagent is effective for direct immunofluorescence staining of human tissue for flow cytometric analysis using 5 µl/10^6 cells.

Comment:

Mouse Monoclonal Anti-Human Lambda CFTMBlue is recommended for use in flow cytometry for identification of Lamba immunoglobulin light chain, to study the presence and extent of clonal expansion in B-lymphoproliferative disorders. Abnormal kappa/lambda ratios or intensities are strong indicators of clonal processes. CF405M (Abs/Em Max: 408/450 nm) US patent application no. 12/607, 915 Direct replacement for: Pacific Blue dye-, BD HorizonTM V450).

Sample Collection: 1. Transfer 100 µl of anticoagulated (EDTA) blood to a 12 x 75 mm polystyrene test tube. 2. Add 2 ml 0.01 mol/l PBS ( It better that it containing 2% bovine serum albumin) and resuspend the cells by using a vortex mixer. 3. Centrifuge at 400 x g for 5 minutes. Gently aspirate the supernatant and discard it leaving approximately 50 µl of fluid. 4. Add 2 ml 0.01 mol/l PBS ( It better that it containing 2% bovine serum albumin) and resuspend the cells by using a vortex mixer. 5. Centrifuge at 400 x g for 5 minutes. Gently aspirate the supernatant and discard it leaving approximately 50 µl of fluid. 6. Add 20 µl of Lambda and mix gently with a vortex mixer. The 20 µl is a guideline only, the optimal volume should be determined by the individual laboratory. 7. The recommended negative control is a non-reactive CFBlue-conjugated antibody of the same isotype. 8. Incubate in the dark at room temperature at 4°C for 30 minutes or at room temperature (20-25 °C) for 15 minutes. 9. Add 100 µl of Lysing Solution to each sample and mix gently with a vortex mixer. Incubate for 10 minutes at room temperature in the dark. 10. Centrifuge at 1000 x g for 5 minutes. Gently aspirate the supernatant and discard it leaving approximately 50 µl of fluid. 11. Add 2 ml 0.01 mol/l PBS ( It better that it containing 2% bovine serum albumin) and resuspend the cells by using a vortex mixer. 12. Centrifuge at 1000 x g for 5 minutes. Gently aspirate the supernatant and discard it leaving approximately 50 µl of fluid. 13. Resuspend pellet in an appropriate fluid for flow cytometry, e.g. 0.3 ml PBS. The PBS should contain 1% paraformaldehyde (fixative) if samples are not analysed the same day. Analyse on a flow cytometer or store at 2-8 °C in the dark until analysis. Samples can be run up to 24 hours after lysis.

Restrictions: For Research Use only

Handling

Buffer: The conjugate is provided in liquid form in buffer containing 1% bovine serum albumin (BSA) and 0, 09% Sodium azide, pH 7.2.

Preservative: Sodium azide

Precaution of Use: 1. The device is not intended for clinical use including diagnosis, prognosis, and monitoring of a disease state, and it must not be used in conjunction with patient records or treatment. 2. This product contains Sodium azide (NaN3), a chemical highly toxic in pure form. At product concentrations, though not classified as hazardous, Sodium azide may react with lead and copper plumbing to form highly explosive build-ups of metal azides. Upon disposal, flush with large volumes of water to prevent metal azide build-up in plumbing. 3. As with any product derived from biological sources, proper handling procedures should be used.

Storage: 4 °C

Target Details

Target: lambda

Background: Human immunoglobulins are glycoproteins composed of two disulfide-bonded heavy (H) chain subunits, each of which is linked by interchain disulfide bonds to a light (L) chain forming a tetramolecular complex. There are five classes of immunoglobulins, designated IgG, IgA, IgM, IgD and IgE, which are defined by differences in the constant region of H chains. L chains are divided into kappa or lambda classifications based on structural antigenic differences. All classes of immunoglobulins have been found on the cell surface of B lymphocytes where they function as antigen receptors to elicit antigen- dependent proliferation and secretion of antigen specific soluble circulating antibodies.