Actin Antikörper (FITC)

Antigen: Actin

Synonyme: A, Ac5C, Act, Actin, Actin/BAP47, Actin5C, BAP47, M32055, T11, act 5C, act5C, actin-5C, anon-EST:fe2D2, beta-actin/Bap47, cyt5C, l(1)G0009, l(1)G0010, l(1)G0025, l(1)G0079, l(1)G0117, l(1)G0177, l(1)G0245, l(1)G0330, l(1)G0420, l(1)G0486, DmelCG4027, CG4027, Act57A, Act57b, BEST:RE38067, C, CG30294, M, T10, act 57A, anon-EST:CL2c12, DmelCG10067, CG10067, 143060_f_at, D, act 79B, act79B, mus79B, DmelCG7478, CG7478, Act(88F), Act88-F, E, Ifm(3)7, act 88F, act88F, rsd, DmelCG5178, CG5178, act 87E, act87E, mus87E, DmelCG18290, CG18290, ACTIN, ACTIN-12, actin, dsim_GLEANR_2829, DsimGD19025, GD19025, Act88F, AFFX-Dros-ACTIN_M_r_at, Act42a, act 42A, DmelCG12051, CG12051

Klonalität: Polyklonal

Wirt: Maus

Reaktivität: Huhn, Ziege, Hamster, Human, Maus, Kaninchen, Ratte (Rattus), Schaf, Xenopus laevis

Konjugat: FITC

Applikation: Immunhistochemie (Gefrierschnitte) (IHC (fro)), Immunfluoreszenz (IF), Immunhistochemie (Paraffinschnitte) (IHC (p))

Produktnummer: ABIN144429

Produktbeschreibung

Weitere Bezeichnung: Actin (pan)

Immunogen: Synthetic peptide: SGPSIVHRKCF (human) attached to a Multiple Antigen Peptide (MAP) backbone.

Isotyp: IgG2a

Beschreibung: The two major cytoskeletal proteins implicated in cell motility are actin and myosin. Actin and myosin are constituents of many cell types and are involved in a myriad of cellular processes including locomotion, secretion, cytoplasmic streaming, phagocytosis and cytokinesis. Although actin is one of the most conserved eukaryotic proteins, it is expressed in mammals and birds as at least six isoforms characterized by electrophoresis and amino acid sequence analysis. Four of them represent the differentiation markers of muscle tissues and two are found in practically all cells.

Spezifität: This antibody does not recognise the epitope on the N-terminal end of actin.

Synonyme: A, Ac5C, Act, Actin, Actin/BAP47, Actin5C, BAP47, M32055, T11, act 5C, act5C, actin-5C, anon-EST:fe2D2, beta-actin/Bap47, cyt5C, l(1)G0009, l(1)G0010, l(1)G0025, l(1)G0079, l(1)G0117, l(1)G0177, l(1)G0245, l(1)G0330, l(1)G0420, l(1)G0486, DmelCG4027, CG4027, Act57A, Act57b, BEST:RE38067, C, CG30294, M, T10, act 57A, anon-EST:CL2c12, DmelCG10067, CG10067, 143060_f_at, D, act 79B, act79B, mus79B, DmelCG7478, CG7478, Act(88F), Act88-F, E, Ifm(3)7, act 88F, act88F, rsd, DmelCG5178, CG5178, act 87E, act87E, mus87E, DmelCG18290, CG18290, ACTIN, ACTIN-12, actin, dsim_GLEANR_2829, DsimGD19025, GD19025, Act88F, AFFX-Dros-ACTIN_M_r_at, Act42a, act 42A, DmelCG12051, CG12051

Anwendungen

Applikationshinweise: IF: Use at a dilution of 1/50 (determined by direct immunofluorescent labeling of cultured human fibroblasts). The conjugate is suitable for dual immunofluorescent staining procedures. IHC-P: Use at an assay dependent dilution. IHC-Fr: Use at an assay dependent dilution. Direct Immunofluorescent Labeling of Cultured Cells:Materials:1. Coverslips.2. Cells (e.g., human or chicken fibroblasts) in DMEM medium + 10% Fetal Calf Serum 3. 10 mM phosphate buffered saline (PBS), pH 7.2-7.4, without preservative 4. PBS containing 1% BSA (diluent).5. Absolute methanol cooled to 20 °,C.6. Acetone, Analytical grade, cooled to 20 °,C (1:1 v/v).7. Aqueous mounting medium.8. Test antibody conjugateCell Growth and Fixation:1. Collect cells from tissue culture dish at a stage of almost confluency, wash with medium and seed on to coverslips. Seed 1-2 x 10^4 cells per cover slip and grow cells in incubator for 2-3 days. Do not change medium.2. Remove coverslips from incubator, discard medium.3. Wash twice with PBS, remove solution by aspiration.4. Add enough cold methanol to cover the cell layer. Incubate 10 minutes at 20 °,C. Aspirate solution.5. Cover cell layer with cold acetone. Incubate 1 minute at 20 °,C. Aspirate solution.6. Wash twice with PBS. Rehydrate in PBS for at least 30 minutes prior to labeling with antibody. Test:1. Dilute Monoclonal Anti-Actin FITC Conjugate 1:50 in PBS containing 1% BSA (diluent). Add enough diluted antibody to cover the cell layer and incubate coverslip for 60 minutes at room temperature.2. Wash 3 times with PBS, 5 minutes each.3. Drain excess solution by touching edge of coverslip on paper toweling.4. Invert onto mounting medium applied on glass slides.5. Read under the UV fluorescence microscope. Mounted preparations can be stored in the dark at 2-8 °,C. Note:1. Do not allow cell layer to dry out at any time during the procedure.2. In case of excessive background staining remove aggregates from the labeled reagent (conjugate) by centrifuging for 15 minutes immediately prior to use. The antibody can be used for staining of methanol-fixed, frozen sections. The epitope recognized by the antibody is resistant to formalin fixation and paraffin-embedding. The conjugate may also be used for the localization of actin using direct immunofluorescent staining of frozen or fixed tissue sections and cultured cells. Not tested in other applications. Optimal dilutions/concentrations should be determined by the end user.

Reinheit: Protein A purified

Buffer: Preservative: 15mM Sodium AzideConstituents: 1% BSA, 0.01M PBS. pH 7.4

Forschungsgebiet: Extrazelluläre Matrix

Beschränkungen: Nur für Forschungszwecke einsetzbar