ba1001  (Boster Bio)


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    Structured Review

    Boster Bio ba1001
    Ba1001, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ba1001/product/Boster Bio
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    ba1001 - by Bioz Stars, 2022-07
    94/100 stars

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    Boster Bio goat anti mouse igg biotin
    The changes in the distribution and numbers of <t>IgA-</t> and <t>IgG-secreting</t> cells in the nasal mucosa (A, C) and trachea (B, D). Results are presented as the mean ± SEM. The level of significance is identified by the P value. Capital letters indicate differences at P
    Goat Anti Mouse Igg Biotin, supplied by Boster Bio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti mouse igg biotin/product/Boster Bio
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    goat anti mouse igg biotin - by Bioz Stars, 2022-07
    96/100 stars
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    The changes in the distribution and numbers of IgA- and IgG-secreting cells in the nasal mucosa (A, C) and trachea (B, D). Results are presented as the mean ± SEM. The level of significance is identified by the P value. Capital letters indicate differences at P

    Journal: The Journal of Veterinary Medical Science

    Article Title: Comparison of immune responses to intranasal and intrapulmonary vaccinations with the attenuated Mycoplasma hyopneumoniae 168 strain in pigs

    doi: 10.1292/jvms.14-0123

    Figure Lengend Snippet: The changes in the distribution and numbers of IgA- and IgG-secreting cells in the nasal mucosa (A, C) and trachea (B, D). Results are presented as the mean ± SEM. The level of significance is identified by the P value. Capital letters indicate differences at P

    Article Snippet: Immunohistochemical examination for IgA- and IgG-secreting cells : The experimental process was the same as that above, except that the mouse anti-porcine CD4 (or CD8) antibody was replaced with a rabbit anti-porcine IgA (or IgG) antibody and the goat anti-mouse IgG-Biotin was replaced with staphylococcal protein A-horseradish peroxidase (SPA-HRP).

    Techniques:

    Identification of lncRNA SMARCD3-OT1 and the expression pattern of SMARCD3-OT1 . ( a ) Results of SMARCD3-OT1 5′ RACE and 3′RACE. ( b ) Schematic image of the locations for SMARCD3-OT1 (red and blue) and SMARCD3X4 (red and black). Arrows represent the direction of transcription. ( c ) Prediction of the SMARCD3-OT1 protein-coding ability. ( d ) Western blotting with anti-EGFP. ( e ) Diagram of the EGFP fusion construct vectors used for transfection. The initiation codon ATGGTG of the EGFP (EGFP wt) gene is mutated to ATTGTT (EGFP mut), and the termination codon TGA of ORFs is mutated to TGG. ( f , g ) RNA sequencing result of SMARCD3-OT1 and further qRT-PCR verification. ( h ) Expression levels of SMARCD3-OT1 in CPMs cultured in growth medium at 50% and 100% cell confluency (50%GM and 100%GM) and differentiation medium from 1 to 5 days (DM1 to DM5) ( n = 6). ( i ) Tissue expression profiles of SMARCD3-OT1 in 7-week-old chickens ( n = 6). ( j ) Expression levels of SMARCD3-OT1 from E10 to E15 ( n = 6). ( k , l ) Distribution of SMARCD3-OT1 in the cytoplasm and nuclei of CPMs was determined by PCR and qRT-PCR. Data are presented as mean ± SEM. Statistical significance of differences between means was assessed using an independent sample t test (* p

    Journal: International Journal of Molecular Sciences

    Article Title: LncRNA SMARCD3-OT1 Promotes Muscle Hypertrophy and Fast-Twitch Fiber Transformation via Enhancing SMARCD3X4 Expression

    doi: 10.3390/ijms23094510

    Figure Lengend Snippet: Identification of lncRNA SMARCD3-OT1 and the expression pattern of SMARCD3-OT1 . ( a ) Results of SMARCD3-OT1 5′ RACE and 3′RACE. ( b ) Schematic image of the locations for SMARCD3-OT1 (red and blue) and SMARCD3X4 (red and black). Arrows represent the direction of transcription. ( c ) Prediction of the SMARCD3-OT1 protein-coding ability. ( d ) Western blotting with anti-EGFP. ( e ) Diagram of the EGFP fusion construct vectors used for transfection. The initiation codon ATGGTG of the EGFP (EGFP wt) gene is mutated to ATTGTT (EGFP mut), and the termination codon TGA of ORFs is mutated to TGG. ( f , g ) RNA sequencing result of SMARCD3-OT1 and further qRT-PCR verification. ( h ) Expression levels of SMARCD3-OT1 in CPMs cultured in growth medium at 50% and 100% cell confluency (50%GM and 100%GM) and differentiation medium from 1 to 5 days (DM1 to DM5) ( n = 6). ( i ) Tissue expression profiles of SMARCD3-OT1 in 7-week-old chickens ( n = 6). ( j ) Expression levels of SMARCD3-OT1 from E10 to E15 ( n = 6). ( k , l ) Distribution of SMARCD3-OT1 in the cytoplasm and nuclei of CPMs was determined by PCR and qRT-PCR. Data are presented as mean ± SEM. Statistical significance of differences between means was assessed using an independent sample t test (* p

    Article Snippet: Goat Anti-rabbit IgG-HRP (BA1054; Boster, Wuhan, China; 1:10,000) and Peroxidase-goat Anti-mouse IgG (BA1051; Boster, Wuhan, China; 1:10,000) were utilized as secondary antibodies.

    Techniques: Expressing, Western Blot, Construct, Transfection, RNA Sequencing Assay, Quantitative RT-PCR, Cell Culture, Polymerase Chain Reaction