goat anti-rabbit igg alkaline phosphatase antibody Search Results


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  • 99
    Millipore alkaline phosphatase conjugated goat anti rabbit
    Alkaline Phosphatase Conjugated Goat Anti Rabbit, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 178 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Vector Laboratories goat antirabbit
    Goat Antirabbit, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 408 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Vector Laboratories alkaline phosphatase conjugated goat anti rabbit antibody
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Antibody, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore goat anti rabbit igg alkaline phosphatase antibody
    Goat Anti Rabbit Igg Alkaline Phosphatase Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Abcam alkaline phosphatase conjugated goat anti rabbit igg secondary antibody
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Igg Secondary Antibody, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 188 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore goat anti rabbit igg alkaline phosphatase conjugate
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Goat Anti Rabbit Igg Alkaline Phosphatase Conjugate, supplied by Millipore, used in various techniques. Bioz Stars score: 91/100, based on 230 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Bio-Rad goat anti rabbit igg antibody conjugated to alkaline phosphatase
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Goat Anti Rabbit Igg Antibody Conjugated To Alkaline Phosphatase, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Novus Biologicals goat anti rabbit igg h l secondary antibody alkaline phosphatase
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Goat Anti Rabbit Igg H L Secondary Antibody Alkaline Phosphatase, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 99/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    SouthernBiotech alkaline phosphatase linked goat anti rabbit igg antibody
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Alkaline Phosphatase Linked Goat Anti Rabbit Igg Antibody, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 92/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology goat anti rabbit igg antibody alkaline phosphatase conjugate
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Goat Anti Rabbit Igg Antibody Alkaline Phosphatase Conjugate, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Bethyl goat anti rabbit igg alkaline phosphatase conjugated antibody
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Goat Anti Rabbit Igg Alkaline Phosphatase Conjugated Antibody, supplied by Bethyl, used in various techniques. Bioz Stars score: 97/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    The Jackson Laboratory alkaline phosphatase conjugated goat anti rabbit igg antibody
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Igg Antibody, supplied by The Jackson Laboratory, used in various techniques. Bioz Stars score: 91/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher alkaline phosphatase conjugated goat anti rabbit immunoglobulin g antibody
    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a <t>polyclonal</t> antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit <t>IgG</t> antibody were present only in the conidial cytoplasm of BbV28.
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Immunoglobulin G Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 91/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore alkaline phosphatase conjugated goat anti rabbit igg antibodies
    Immunolocalization of expressed S. litura <t>APN.</t> Surface expression of the APN was examined at 36 h postinfection by immunofluorescence staining with rabbit polyclonal antibodies raised against APN and FITC-conjugated goat anti-rabbit <t>IgG.</t> (A) Cells overlaid with preimmune serum. (B) Cells overlaid with anti-APN antibodies.
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Igg Antibodies, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 25 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega alkaline phosphatase conjugated goat anti rabbit igg antibody
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Igg Antibody, supplied by Promega, used in various techniques. Bioz Stars score: 92/100, based on 35 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology alkaline phosphatase conjugated goat anti rabbit immunoglobulin g antibody
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Immunoglobulin G Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega secondary antibody goat anti rabbit igg alkaline phosphatase ap
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Secondary Antibody Goat Anti Rabbit Igg Alkaline Phosphatase Ap, supplied by Promega, used in various techniques. Bioz Stars score: 85/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Abcam goat anti rabbit igg conjugated alkaline phosphatase antibody
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Goat Anti Rabbit Igg Conjugated Alkaline Phosphatase Antibody, supplied by Abcam, used in various techniques. Bioz Stars score: 86/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    AnaSpec alkaline phosphatase conjugated goat anti rabbit igg antibody
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Alkaline Phosphatase Conjugated Goat Anti Rabbit Igg Antibody, supplied by AnaSpec, used in various techniques. Bioz Stars score: 91/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore rabbit anti goat secondary conjugated to alkaline phosphatase
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Rabbit Anti Goat Secondary Conjugated To Alkaline Phosphatase, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 39 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Antibodies-Online Inc secondary antibody goat anti rabbit igg alkaline phosphatase secondary
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Secondary Antibody Goat Anti Rabbit Igg Alkaline Phosphatase Secondary, supplied by Antibodies-Online Inc, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore alkaline phosphatase labeled goat anti rabbit igg antibody
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Alkaline Phosphatase Labeled Goat Anti Rabbit Igg Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 92/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    PerkinElmer goat anti rabbit igg antibody conjugated to alkaline phosphatase ap
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Goat Anti Rabbit Igg Antibody Conjugated To Alkaline Phosphatase Ap, supplied by PerkinElmer, used in various techniques. Bioz Stars score: 85/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    Millipore goat anti rabbit igg whole molecule conjugated to alkaline phosphatase
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Goat Anti Rabbit Igg Whole Molecule Conjugated To Alkaline Phosphatase, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega alkaline phosphatase labeled goat anti rabbit igg antibody
    <t>α-AgAPN1</t> PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 <t>IgG</t> and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P
    Alkaline Phosphatase Labeled Goat Anti Rabbit Igg Antibody, supplied by Promega, used in various techniques. Bioz Stars score: 88/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Zhongshan Golden Bridge Company goat anti rabbit igg antibody conjugated to alkaline phosphatase
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    Image Search Results


    Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a polyclonal antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit IgG antibody were present only in the conidial cytoplasm of BbV28.

    Journal: Applied and Environmental Microbiology

    Article Title: Integration of Insecticidal Protein Vip3Aa1 into Beauveria bassiana Enhances Fungal Virulence to Spodoptera litura Larvae by Cuticle and PerOs Infection ▿

    doi: 10.1128/AEM.00302-10

    Figure Lengend Snippet: Evidence for Vip3Aa1 expression in transgenic (BbV28) and wild-type (BbW) B. bassiana strains. (a) RT-PCR detection of vip3Aa1 transcription in BbV28 and BbW (negative control). (b) Western blot analysis with a polyclonal antibody against Vip3Aa1. Lanes 1 and 3, protein extracts from BbW mycelia and conidia, respectively; lanes 2 and 4, protein extracts from BbV28 mycelia and conidia, respectively; lanes 5 and 6, lysates of E. coli cells expressing His 6 -tagged Vip3Aa1 (positive control) and of cells vectoring an empty plasmid, respectively; lane M, molecular size marker. (c) Immunogold localization of Vip3Aa1 expressed in aerial conidia of BbV28. (1) BbW integrated only with empty plasmid pAN52-Bar (blank control); (2) BbW (negative control); (3) BbV28 expressing Vip3Aa1. Note that dense 10-nm colloidal gold particles (expressing Vip3Aa1) labeled with the polyclonal antibody and a goat anti-rabbit IgG antibody were present only in the conidial cytoplasm of BbV28.

    Article Snippet: All blots were probed with a 1,000× dilution of the polyclonal antibody and were visualized with goat anti-rabbit IgG-alkaline phosphatase conjugate (Novagen).

    Techniques: Expressing, Transgenic Assay, Reverse Transcription Polymerase Chain Reaction, Negative Control, Western Blot, Positive Control, Plasmid Preparation, Marker, Labeling

    Immunolocalization of expressed S. litura APN. Surface expression of the APN was examined at 36 h postinfection by immunofluorescence staining with rabbit polyclonal antibodies raised against APN and FITC-conjugated goat anti-rabbit IgG. (A) Cells overlaid with preimmune serum. (B) Cells overlaid with anti-APN antibodies.

    Journal: Applied and Environmental Microbiology

    Article Title: Interaction of Gene-Cloned and Insect Cell-Expressed Aminopeptidase N of Spodoptera litura with Insecticidal Crystal Protein Cry1C

    doi: 10.1128/AEM.68.9.4583-4592.2002

    Figure Lengend Snippet: Immunolocalization of expressed S. litura APN. Surface expression of the APN was examined at 36 h postinfection by immunofluorescence staining with rabbit polyclonal antibodies raised against APN and FITC-conjugated goat anti-rabbit IgG. (A) Cells overlaid with preimmune serum. (B) Cells overlaid with anti-APN antibodies.

    Article Snippet: The membrane was incubated with anti-APN antibodies followed by alkaline phosphatase conjugated goat anti-rabbit IgG antibodies and developed with NBT-BCIP.

    Techniques: Expressing, Immunofluorescence, Staining

    Ligand blot analysis of insect cells expressing S. litura APN. Membrane proteins (2.5 μg) prepared from uninfected Sf21 cells (lane 1) and BV-SlApn-infected cells (lane 2 and 3) were solubilized in SDS sample buffer containing β-mercaptoethanol, separated by SDS-7.5% PAGE, and electrotransferred to nitrocellulose membrane. The nitrocellulose membrane was probed with Cry1C (1 μg/ml) (lanes 1 and 2) and Cry1Ac (1 μg/ml) (lane 3) δ-endotoxins. Binding of the toxin was detected by using antibodies against the toxin followed by alkaline phosphatase-conjugated goat anti-rabbit IgG. The positions of molecular mass markers (in kilodaltons) are indicated on the left.

    Journal: Applied and Environmental Microbiology

    Article Title: Interaction of Gene-Cloned and Insect Cell-Expressed Aminopeptidase N of Spodoptera litura with Insecticidal Crystal Protein Cry1C

    doi: 10.1128/AEM.68.9.4583-4592.2002

    Figure Lengend Snippet: Ligand blot analysis of insect cells expressing S. litura APN. Membrane proteins (2.5 μg) prepared from uninfected Sf21 cells (lane 1) and BV-SlApn-infected cells (lane 2 and 3) were solubilized in SDS sample buffer containing β-mercaptoethanol, separated by SDS-7.5% PAGE, and electrotransferred to nitrocellulose membrane. The nitrocellulose membrane was probed with Cry1C (1 μg/ml) (lanes 1 and 2) and Cry1Ac (1 μg/ml) (lane 3) δ-endotoxins. Binding of the toxin was detected by using antibodies against the toxin followed by alkaline phosphatase-conjugated goat anti-rabbit IgG. The positions of molecular mass markers (in kilodaltons) are indicated on the left.

    Article Snippet: The membrane was incubated with anti-APN antibodies followed by alkaline phosphatase conjugated goat anti-rabbit IgG antibodies and developed with NBT-BCIP.

    Techniques: Expressing, Infection, Polyacrylamide Gel Electrophoresis, Binding Assay

    Differential toxin binding to surface-expressed S. litura APN. Sf21 cells infected for 36 h were overlaid with Cry1Ac (A) or Cry1C (B) toxin (1 μg/ml). Binding of the toxin was detected by using antibodies against the toxin followed by FITC-conjugated goat anti-rabbit IgG.

    Journal: Applied and Environmental Microbiology

    Article Title: Interaction of Gene-Cloned and Insect Cell-Expressed Aminopeptidase N of Spodoptera litura with Insecticidal Crystal Protein Cry1C

    doi: 10.1128/AEM.68.9.4583-4592.2002

    Figure Lengend Snippet: Differential toxin binding to surface-expressed S. litura APN. Sf21 cells infected for 36 h were overlaid with Cry1Ac (A) or Cry1C (B) toxin (1 μg/ml). Binding of the toxin was detected by using antibodies against the toxin followed by FITC-conjugated goat anti-rabbit IgG.

    Article Snippet: The membrane was incubated with anti-APN antibodies followed by alkaline phosphatase conjugated goat anti-rabbit IgG antibodies and developed with NBT-BCIP.

    Techniques: Binding Assay, Infection

    α-AgAPN1 PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 IgG and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Disruption of Plasmodium falciparum development by antibodies against a conserved mosquito midgut antigen

    doi: 10.1073/pnas.0702239104

    Figure Lengend Snippet: α-AgAPN1 PAbs block P. berghei and P. falciparum development in mosquitoes. ( a ) α-AgAPN1 IgG and Fab fragments inhibit oocyst development in mosquitoes. A. gambiae mosquitoes were fed on P. berghei -infected mice that were passively immunized (i.v.) with α-AgAPN1 IgG or Fab. Numbers of mosquitoes analyzed are shown in the bottom of each column. Pooled data from three replicate experiments are shown. Asterisks denote significance values of P

    Article Snippet: Transblots were probed with α-AgAPN1 PAbs (1:500) followed by alkaline phosphatase-conjugated goat anti-rabbit IgG secondary antibody (Promega, Madison, WI) and detection with CDP-Star substrate (PerkinElmer, Wellesley, MA).

    Techniques: Blocking Assay, Infection, Mouse Assay

    Specific blocking of Fc receptors on J774A.1 cells abrogates the inhibition of YopH delivery by anti-LcrV antibody. Panel A: control test for efficacy of FcBlock in inhibiting phagocytosis mediated by IgG1. J774A.1 cells were treated with Fc Block or

    Journal: Infection and Immunity

    Article Title: Anti-LcrV Antibody Inhibits Delivery of Yops by Yersinia pestis KIM5 by Directly Promoting Phagocytosis

    doi: 10.1128/IAI.73.9.6127-6137.2005

    Figure Lengend Snippet: Specific blocking of Fc receptors on J774A.1 cells abrogates the inhibition of YopH delivery by anti-LcrV antibody. Panel A: control test for efficacy of FcBlock in inhibiting phagocytosis mediated by IgG1. J774A.1 cells were treated with Fc Block or

    Article Snippet: Their functionality was demonstrated in an immunoblot in which hexahistidine-tagged LcrV on the blot was probed with F(ab′)2 fragments or full-length anti-LcrV antibody, detected with alkaline-phosphatase-conjugated goat anti-rabbit IgG heavy plus light chains (Bethyl), and developed with Nitro Blue Tetrazolium - BCIP (5-bromo-4-chloro-3-indolylphosphate) (Sigma-Aldrich).

    Techniques: Blocking Assay, Inhibition