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rabbit anti human α 6 integrin subunit  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit anti human α 6 integrin subunit
    Immunohistochemistry with antibodies to CD151, HER-2, integrins α 6 β 1, α 3 β 1 and E-cadherin. A and B – CD151 ( × 100 and × 200, respectively); C and D – E-cadherin ( × 100 and × 200, respectively); E and F – <t>integrin</t> α 3 β 1 ( × 100 and × 200, respectively); G and H – integrin α 6 β 1 ( × 100 and × 200, respectively).
    Rabbit Anti Human α 6 Integrin Subunit, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 4704 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/integrin+%CE%B1+6+subunit/pmc03101917-116-29-35?v=Santa+Cruz+Biotechnology
    Average 96 stars, based on 4704 article reviews
    rabbit anti human α 6 integrin subunit - by Bioz Stars, 2026-07
    96/100 stars

    Images

    1) Product Images from "Tetraspanin CD151 is a novel prognostic marker in poor outcome endometrial cancer"

    Article Title: Tetraspanin CD151 is a novel prognostic marker in poor outcome endometrial cancer

    Journal: British Journal of Cancer

    doi: 10.1038/bjc.2011.80

    Immunohistochemistry with antibodies to CD151, HER-2, integrins α 6 β 1, α 3 β 1 and E-cadherin. A and B – CD151 ( × 100 and × 200, respectively); C and D – E-cadherin ( × 100 and × 200, respectively); E and F – integrin α 3 β 1 ( × 100 and × 200, respectively); G and H – integrin α 6 β 1 ( × 100 and × 200, respectively).
    Figure Legend Snippet: Immunohistochemistry with antibodies to CD151, HER-2, integrins α 6 β 1, α 3 β 1 and E-cadherin. A and B – CD151 ( × 100 and × 200, respectively); C and D – E-cadherin ( × 100 and × 200, respectively); E and F – integrin α 3 β 1 ( × 100 and × 200, respectively); G and H – integrin α 6 β 1 ( × 100 and × 200, respectively).

    Techniques Used: Immunohistochemistry



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    Image Search Results


    Antibodies, commercial sources, and applications.

    Journal: Neuroscience Journal

    Article Title: Roles of Integrins and Intracellular Molecules in the Migration and Neuritogenesis of Fetal Cortical Neurons: MEK Regulates Only the Neuritogenesis

    doi: 10.1155/2013/859257

    Figure Lengend Snippet: Antibodies, commercial sources, and applications.

    Article Snippet: Monoclonal antibodies against α 6 integrin subunit (Clone NKI-GoH3) , BD Biosciences , Migration assays.

    Techniques: Migration, Microscopy, Western Blot, Purification, Immunofluorescence

    Primers used for the amplification of  integrin  cDNA from rat fetal brain neurons.

    Journal: Neuroscience Journal

    Article Title: Roles of Integrins and Intracellular Molecules in the Migration and Neuritogenesis of Fetal Cortical Neurons: MEK Regulates Only the Neuritogenesis

    doi: 10.1155/2013/859257

    Figure Lengend Snippet: Primers used for the amplification of integrin cDNA from rat fetal brain neurons.

    Article Snippet: Monoclonal antibodies against α 6 integrin subunit (Clone NKI-GoH3) , BD Biosciences , Migration assays.

    Techniques: Amplification

    Effects of antibodies, calcium modulators, and pharmacological inhibitors on neuritogenesis. (a) Representative images showing neuritogenesis in the absence (control) or presence of control IgG (50 nMole), antibodies against β 1 (50 or 100 nMole) or α 3 (50 or 100 nMole) integrin subunits on laminin. BAPTA-AM at low concentration (2.5 μ M) inhibited neuritogenesis and at higher concentration (10 μ M) totally abolished neuritogenesis. Bar150 microns. (b) Mean + standard error of mean values of neurite lengths/image in untreated neurons (1) and those treated with control IgG, monoclonal antibody against β 1 or α 3 integrin subunit at 50 nMole or 100 nMole concentration. Neurite lengths reduced significantly ( * P < 0.05) in neurons treated with antibody against β 1 integrin subunit at both 50 nMole (2) and 100 nMole (3) concentrations compared to control (1). Neurons treated with monoclonal antibody against α 3 integrin subunit at 50 nMole (4) were lower than the control (1) but was not statistically significant ( P > 0.05). Neurons treated with monoclonal antibody against α 3 integrin subunit at 100 nMole (5) significantly inhibited the neuritogenesis ( * P < 0.055). Neuritogenesis was not altered in presence of 50 (6) or 100 nMole (7) control IgG ( P > 0.05). (c) Mean + standard error of mean values of neurite lengths/image of neurons treated with PP2, PP3, U2, U3, 2-APB, activated Calphostin, BAPTA-AM (2.5 μ M), and PD for 22 h in culture (filled bars) were significantly different ( * P < 0.05) from untreated neurons (blank bar) and negative controls (PP3 or U3) (filled bars). No significant changes in neurite lengths ( P > 0.05) per image were recorded in neurons treated with RR.

    Journal: Neuroscience Journal

    Article Title: Roles of Integrins and Intracellular Molecules in the Migration and Neuritogenesis of Fetal Cortical Neurons: MEK Regulates Only the Neuritogenesis

    doi: 10.1155/2013/859257

    Figure Lengend Snippet: Effects of antibodies, calcium modulators, and pharmacological inhibitors on neuritogenesis. (a) Representative images showing neuritogenesis in the absence (control) or presence of control IgG (50 nMole), antibodies against β 1 (50 or 100 nMole) or α 3 (50 or 100 nMole) integrin subunits on laminin. BAPTA-AM at low concentration (2.5 μ M) inhibited neuritogenesis and at higher concentration (10 μ M) totally abolished neuritogenesis. Bar150 microns. (b) Mean + standard error of mean values of neurite lengths/image in untreated neurons (1) and those treated with control IgG, monoclonal antibody against β 1 or α 3 integrin subunit at 50 nMole or 100 nMole concentration. Neurite lengths reduced significantly ( * P < 0.05) in neurons treated with antibody against β 1 integrin subunit at both 50 nMole (2) and 100 nMole (3) concentrations compared to control (1). Neurons treated with monoclonal antibody against α 3 integrin subunit at 50 nMole (4) were lower than the control (1) but was not statistically significant ( P > 0.05). Neurons treated with monoclonal antibody against α 3 integrin subunit at 100 nMole (5) significantly inhibited the neuritogenesis ( * P < 0.055). Neuritogenesis was not altered in presence of 50 (6) or 100 nMole (7) control IgG ( P > 0.05). (c) Mean + standard error of mean values of neurite lengths/image of neurons treated with PP2, PP3, U2, U3, 2-APB, activated Calphostin, BAPTA-AM (2.5 μ M), and PD for 22 h in culture (filled bars) were significantly different ( * P < 0.05) from untreated neurons (blank bar) and negative controls (PP3 or U3) (filled bars). No significant changes in neurite lengths ( P > 0.05) per image were recorded in neurons treated with RR.

    Article Snippet: Monoclonal antibodies against α 6 integrin subunit (Clone NKI-GoH3) , BD Biosciences , Migration assays.

    Techniques: Concentration Assay

    Transcripts of integrin subunits in the fetal cortical neurons. Ethidium bromide stained PCR products after agarose gel electrophoresis. Target mRNA species are shown at the bottom of the image. The 600 bp band of the 100 bp marker (M) is shown by arrows heads on sides.

    Journal: Neuroscience Journal

    Article Title: Roles of Integrins and Intracellular Molecules in the Migration and Neuritogenesis of Fetal Cortical Neurons: MEK Regulates Only the Neuritogenesis

    doi: 10.1155/2013/859257

    Figure Lengend Snippet: Transcripts of integrin subunits in the fetal cortical neurons. Ethidium bromide stained PCR products after agarose gel electrophoresis. Target mRNA species are shown at the bottom of the image. The 600 bp band of the 100 bp marker (M) is shown by arrows heads on sides.

    Article Snippet: Monoclonal antibodies against α 6 integrin subunit (Clone NKI-GoH3) , BD Biosciences , Migration assays.

    Techniques: Staining, Agarose Gel Electrophoresis, Marker

    Effects of antibodies on the migration of fetal cortical neurons. Monoclonal antibodies (shown below) against β 1 and α 3 integrin subunits significantly ( * P < 0.05) inhibited the migration of neurons (Neurons/field) on membranes coated with laminin (10 μ g/mL) (a). The migrations of neurons on laminin-coated membranes were not significantly ( P > 0.05) altered by antibody against α 6 or αv subunit (the negative control) and control antibodies (IgG or IgM). The migrations of neurons on fibronectin (100 μ g/mL) coated membranes were significantly ( * P < 0.05) inhibited by the antibody against β 1 integrin subunit only (b). The migrations of neurons on fibronectin-coated membranes were not altered by control antibodies (IgG or IgM) at P > 0.05.

    Journal: Neuroscience Journal

    Article Title: Roles of Integrins and Intracellular Molecules in the Migration and Neuritogenesis of Fetal Cortical Neurons: MEK Regulates Only the Neuritogenesis

    doi: 10.1155/2013/859257

    Figure Lengend Snippet: Effects of antibodies on the migration of fetal cortical neurons. Monoclonal antibodies (shown below) against β 1 and α 3 integrin subunits significantly ( * P < 0.05) inhibited the migration of neurons (Neurons/field) on membranes coated with laminin (10 μ g/mL) (a). The migrations of neurons on laminin-coated membranes were not significantly ( P > 0.05) altered by antibody against α 6 or αv subunit (the negative control) and control antibodies (IgG or IgM). The migrations of neurons on fibronectin (100 μ g/mL) coated membranes were significantly ( * P < 0.05) inhibited by the antibody against β 1 integrin subunit only (b). The migrations of neurons on fibronectin-coated membranes were not altered by control antibodies (IgG or IgM) at P > 0.05.

    Article Snippet: Monoclonal antibodies against α 6 integrin subunit (Clone NKI-GoH3) , BD Biosciences , Migration assays.

    Techniques: Migration, Negative Control

    Schematic of integrin signaling cascade and its perturbation with antibodies and pharmacological agents. Integrin subunits (red and green bars on top) are shown intercalated in the membrane and interacting with ECM molecule (red and green horizontal lines). Molecules involved in signaling events are labeled and arrows point to the directions of signaling that starts with the engagement of integrin subunit with the extracellular matrix. Directions of calcium mediated signaling are shown by dashed green arrows. Inhibitors (see ) used for blocking signaling molecules and paths are shown by red blocks. Cross-talk between integrin and GF signaling is shown by double headed horizontal arrow close to membrane. Mab: monoclonal antibody, GF: growth factor, RTK: receptor tyrosine kinase, MEK: MAP kinase kinase, PLC: phospholipase C, PIP2: phosphotidal inositol biphosphate, IP3: inositol (1,4,5)-triphosphate (IP3), DAG: diacylglycerol and PKC: protein kinase C, Ras: G protein, Raf: MAPKKK, MEK: MAPKK, ERK: extracellular signal regulated kinase (MAPK).

    Journal: Neuroscience Journal

    Article Title: Roles of Integrins and Intracellular Molecules in the Migration and Neuritogenesis of Fetal Cortical Neurons: MEK Regulates Only the Neuritogenesis

    doi: 10.1155/2013/859257

    Figure Lengend Snippet: Schematic of integrin signaling cascade and its perturbation with antibodies and pharmacological agents. Integrin subunits (red and green bars on top) are shown intercalated in the membrane and interacting with ECM molecule (red and green horizontal lines). Molecules involved in signaling events are labeled and arrows point to the directions of signaling that starts with the engagement of integrin subunit with the extracellular matrix. Directions of calcium mediated signaling are shown by dashed green arrows. Inhibitors (see ) used for blocking signaling molecules and paths are shown by red blocks. Cross-talk between integrin and GF signaling is shown by double headed horizontal arrow close to membrane. Mab: monoclonal antibody, GF: growth factor, RTK: receptor tyrosine kinase, MEK: MAP kinase kinase, PLC: phospholipase C, PIP2: phosphotidal inositol biphosphate, IP3: inositol (1,4,5)-triphosphate (IP3), DAG: diacylglycerol and PKC: protein kinase C, Ras: G protein, Raf: MAPKKK, MEK: MAPKK, ERK: extracellular signal regulated kinase (MAPK).

    Article Snippet: Monoclonal antibodies against α 6 integrin subunit (Clone NKI-GoH3) , BD Biosciences , Migration assays.

    Techniques: Labeling, Blocking Assay

    Immunohistochemistry with antibodies to CD151, HER-2, integrins α 6 β 1, α 3 β 1 and E-cadherin. A and B – CD151 ( × 100 and × 200, respectively); C and D – E-cadherin ( × 100 and × 200, respectively); E and F – integrin α 3 β 1 ( × 100 and × 200, respectively); G and H – integrin α 6 β 1 ( × 100 and × 200, respectively).

    Journal: British Journal of Cancer

    Article Title: Tetraspanin CD151 is a novel prognostic marker in poor outcome endometrial cancer

    doi: 10.1038/bjc.2011.80

    Figure Lengend Snippet: Immunohistochemistry with antibodies to CD151, HER-2, integrins α 6 β 1, α 3 β 1 and E-cadherin. A and B – CD151 ( × 100 and × 200, respectively); C and D – E-cadherin ( × 100 and × 200, respectively); E and F – integrin α 3 β 1 ( × 100 and × 200, respectively); G and H – integrin α 6 β 1 ( × 100 and × 200, respectively).

    Article Snippet: Cell surface adhesion molecules goat anti-human α 3 integrin subunit (Santa Cruz, Santa Cruz, CA, USA, sc-6588, antibody concentration 0.67 μ g ml −1 ; dilution 1 : 300), rabbit anti-human α 6 integrin subunit (Santa Cruz, sc-10730, antibody concentration 0.5 μ g ml −1 ; dilution 1 : 400) and mouse anti-E-cadherin (clone NCH-38, Dako (Copenhagen, Denmark), antibody concentration 0.1 μ g ml −1 ; dilution 1 : 2000) were used.

    Techniques: Immunohistochemistry