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              Talin-1 Antibody (YQ-16)

              • 更新時間:  2023-07-25
              • 產品型號:  santacruz SC-81805
              • 簡單描述
              • mouse monoclonal IgG3 provided at 100 µg/ml
                recommended for detection of Talin-1 of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA
              詳細介紹

              SANTA CRUZ BIOTECHNOLOGY, INC.
              Talin-1 (YQ-16): sc-81805
              Santa Cruz Biotechnology, Inc. 1.800.457.3801 831.457.3800 831.457.3801 Europe +00800 4573 8000 49 6221 4503 0 www.scbt.com
              BACKGROUND
              Focal adhesions were identified as areas within the plasma membrane of
              tissue culture cells that adhere tightly to the underlying substrate. In vivo,
              these regions are involved in the adhesion of cells to the extracellular matrix.
              Paxillin and vinculin are cytoskeletal, focal adhesion proteins that are components
              of a protein complex that links the Actin network to the plasma
              membrane. Vinculin binding sites have been identified on other cytoskeletal
              proteins, including Talin-1 and α-actinin. In addition, vinculin, Talin-1, Talin-2
              and α-actinin each contain Actin binding sites. Expression of vinculin, Talin-1
              and Talin-2 have been shown to be affected by the level of Actin expression.
              α-actinin has been shown to link Actin to integrins in the plasma membrane
              through interactions with the vinculin and Talin complex or by a direct interaction
              with integrin. Talin-2 is similar to Talin-1 but shows distinct patterns of
              expression and cannot compensate for the loss of Talin-1.
              REFERENCES
              1. Burridge, K., et al. 1988. Focal adhesions: transmembrane junctions
              between the extracellular matrix and the cytoskeleton. Annu. Rev. Cell
              Biol. 4: 487-525.
              2. Gilmore, A.P., et al. 1992. Further characterization of the Talin-binding site
              in the cytoskeletal protein vinculin. J. Cell Sci. 103: 719-731.
              3.Wood, C.K., et al. 1994. Characterisation of the paxillin-binding site and
              the C-terminal focal adhesion targeting sequence in vinculin. J. Cell Sci.
              107: 709-717.
              4. Gluck, U., et al. 1994. Modulation of α-actinin levels affects cell motility
              and confers tumorigenicity on 3T3 cells. J. Cell Sci. 107: 1773-1782.
              5. Schevzov, G., et al. 1995. Impact of Actin gene expression on vinculin,
              Talin, cell spreading, and motility. DNA Cell Biol. 14: 689-700.
              6. Hemmings, L., et al. 1996. Talin contains three Actin-binding sites each of
              which is adjacent to a vinculin-binding site. J. Cell Sci. 109: 2715-2726.
              7. Gilmore, A.P., et al. 1996. Regulation of vinculin binding to Talin and Actin
              by phosphatidyl-inositol-4-5-bisphosphate. Nature 381: 531-535.
              CHROMOSOMAL LOCATION
              Genetic locus: TLN1 (human) mapping to 9p13.3; Tln1 (mouse) mapping to
              4 B1.
              SOURCE
              Talin-1 (YQ-16) is a mouse monoclonal antibody raised against recombinant
              Talin-1 of human origin.
              PRODUCT
              Each vial contains 100 μg IgG3 in 1.0 ml PBS with < 0.1% sodium azide and
              0.1% gelatin.
              STORAGE
              Store at 4° C, **DO NOT FREEZE**. Stable for one year from the date of
              shipment. Non-hazardous. No MSDS required.
              APPLICATIONS
              Talin-1 (YQ-16) is recommended for detection of Talin-1 of mouse, rat and
              human origin by Western Blotting (starting dilution 1:200, dilution range
              1:100-1:1000), immunoprecipitation [1-2 μg per 100-500 μg of total protein
              (1 ml of cell lysate)], immunofluorescence (starting dilution 1:50, dilution
              range 1:50-1:500), immunohistochemistry (including paraffin-embedded
              sections) (starting dilution 1:50, dilution range 1:50-1:500) and solid phase
              ELISA (starting dilution 1:30, dilution range 1:30-1:3000).
              Suitable for use as control antibody for Talin-1 siRNA (h): sc-36610, Talin-1
              siRNA (m): sc-36611, Talin-1 shRNA Plasmid (h): sc-36610-SH, Talin-1 shRNA
              Plasmid (m): sc-36611-SH, Talin-1 shRNA (h) Lentiviral Particles: sc-36610-V
              and Talin-1 shRNA (m) Lentiviral Particles: sc-36611-V.
              Molecular Weight of Talin-1: 230 kDa.
              Positive Controls: RAW 264.7 whole cell lysate: sc-2211.
              RECOMMENDED SECONDARY REAGENTS
              To ensure optimal results, the following support (secondary) reagents are
              recommended: 1) Western Blotting: use goat anti-mouse IgG-HRP: sc-2005
              (dilution range: 1:2000-1:32,000) or Cruz Marker™ compatible goat antimouse
              IgG-HRP: sc-2031 (dilution range: 1:2000-1:5000), Cruz Marker™
              Molecular Weight Standards: sc-2035, TBS Blotto A Blocking Reagent:
              sc-2333 and Western Blotting Luminol Reagent: sc-2048. 2) Immunoprecipitation:
              use Protein A/G PLUS-Agarose: sc-2003 (0.5 ml agarose/2.0 ml).
              3) Immunofluorescence: use goat anti-mouse IgG-FITC: sc-2010 (dilution
              range: 1:100-1:400) or goat anti-mouse IgG-TR: sc-2781 (dilution range:
              1:100-1:400) with UltraCruz™ Mounting Medium: sc-24941. 4) Immunohistochemistry:
              use ImmunoCruz™: sc-2050 or ABC: sc-2017 mouse IgG
              Staining Systems.
              DATA
              SELECT PRODUCT CITATIONS
              1. Ah Kioon, M.D., et al. 2010. Adrenomedullin increases fibroblast-like synoviocyte
              adhesion to extracellular matrix proteins by upregulating integrin
              activation. Arthritis Res. Ther. 12: R190.
              RESEARCH USE
              For research use only, not for use in diagnostic procedures.

               

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