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lambda mouse 129-sv/j genomic dna library  (Agilent technologies)


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    Agilent technologies lambda mouse 129-sv/j genomic dna library
    Lambda Mouse 129 Sv/J Genomic Dna Library, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/a+lambda+129/pmc03990712-29-18-24
    Average 90 stars, based on 1 article reviews
    lambda mouse 129-sv/j genomic dna library - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Syncoilin is required for generating maximum isometric stress in skeletal muscle but dispensable for muscle cytoarchitecture
    Article Snippet: Genomic DNA clones were isolated from a mouse 129-SVJ genomic DNA library (Stratagene, La Jolla, CA) by screening using a full-length syncoilin probe.

    Article Title: MondoA deficiency enhances sprint performance in mice
    Article Snippet: Using a mouse 129-strain λ genomic library (Stratagene), we isolated clones containing MondoA genomic DNA.

    Article Title: Generation and Characterization of a Mouse Model Harboring the Exon-3 Deletion in the Cardiac Ryanodine Receptor
    Article Snippet: A genomic DNA phage clone containing part of the mouse cardiac ryanodine receptor gene was isolated from the lambda mouse 129-SV/J genomic DNA library (Stratagene) and used to construct the RyR2 exon-3 deletion (Ex3-del) knock-in (KI) targeting vector.

    Article Title: Distribution and Function of Cardiac Ryanodine Receptor Clusters in Live Ventricular Myocytes
    Article Snippet: Generation of a knock-in mouse model expressing a GFP-tagged RyR2 – A genomic DNA phage clone containing part of the mouse cardiac ryanodine receptor gene was isolated from the lambda mouse 129-SV/J genomic DNA library (Stratagene) and used to construct the RyR2 GFP knockin (KI) targeting vector.

    Isolation:

    Article Title: Ankrd2 is a modulator of NF- κ B-mediated inflammatory responses during muscle differentiation
    Article Snippet: .. Genomic DNA was isolated from a mouse 129-SVJ genomic DNA library (Stratagene, La Jolla, CA, USA), using full-length Ankrd2 cDNA as a probe. ..

    Article Title: In Vivo Function and Evolution of the Eutherian-Specific Pluripotency Marker UTF1
    Article Snippet: .. Genomic clones carrying the UTF1 gene were isolated from the mouse 129 SVJ λFixII library (Stratagene). ..

    Article Title: High blood pressure arising from a defect in vascular function
    Article Snippet: .. Phage clones spanning exon1α of PKG1α were isolated from a mouse 129 genomic library (Stratagene) and used to construct a targeting vector according to standard procedures. ..

    Clone Assay:

    Article Title: In Vivo Function and Evolution of the Eutherian-Specific Pluripotency Marker UTF1
    Article Snippet: .. Genomic clones carrying the UTF1 gene were isolated from the mouse 129 SVJ λFixII library (Stratagene). ..

    Article Title: High blood pressure arising from a defect in vascular function
    Article Snippet: .. Phage clones spanning exon1α of PKG1α were isolated from a mouse 129 genomic library (Stratagene) and used to construct a targeting vector according to standard procedures. ..

    Construct:

    Article Title: High blood pressure arising from a defect in vascular function
    Article Snippet: .. Phage clones spanning exon1α of PKG1α were isolated from a mouse 129 genomic library (Stratagene) and used to construct a targeting vector according to standard procedures. ..

    Plasmid Preparation:

    Article Title: High blood pressure arising from a defect in vascular function
    Article Snippet: .. Phage clones spanning exon1α of PKG1α were isolated from a mouse 129 genomic library (Stratagene) and used to construct a targeting vector according to standard procedures. ..



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    Image Search Results


    Human multiple myeloma cell line U266-ffluc was i.v. (tail vein) injected into NSG mice. After 4 weeks, the mice were randomized into 3 groups comprising 8–9 mice each and treated with i.v. (tail vein) injections of 3 mg/kg of the ADC, the unconjugated antibody, and vehicle alone. (A) Human lambda light chain concentrations correlating with tumor burden were determined by ELISA at the indicated time points and plotted as mean ± SD values. The p value (t-test) compares the ADC group to the unconjugated antibody group. (B) Kaplan-Meier survival curve. The p value (log-rank test) compares the ADC group to the unconjugated antibody group. See also Figure S3 and Table S3.

    Journal: Cell chemical biology

    Article Title: Stable and potent selenomab-drug conjugates

    doi: 10.1016/j.chembiol.2017.02.012

    Figure Lengend Snippet: Human multiple myeloma cell line U266-ffluc was i.v. (tail vein) injected into NSG mice. After 4 weeks, the mice were randomized into 3 groups comprising 8–9 mice each and treated with i.v. (tail vein) injections of 3 mg/kg of the ADC, the unconjugated antibody, and vehicle alone. (A) Human lambda light chain concentrations correlating with tumor burden were determined by ELISA at the indicated time points and plotted as mean ± SD values. The p value (t-test) compares the ADC group to the unconjugated antibody group. (B) Kaplan-Meier survival curve. The p value (log-rank test) compares the ADC group to the unconjugated antibody group. See also Figure S3 and Table S3.

    Article Snippet: Human Lambda ELISA Quantitation Set , Bethyl Laboratories , Cat#E80-116.

    Techniques: Injection, Enzyme-linked Immunosorbent Assay

    (A) Human breast cancer cell line KPL-4 was xenografted into the mammary fat pads of female NSG mice, grown to ~150 mm3, randomized into 5 groups comprising 6 mice each, and treated with i.v. (tail vein) injections of the indicated ADCs and controls four times every week at 5 mg/kg. Mean ± SD values are plotted. (B) Four female CD-1 mice were injected i.v. with 6 mg/kg of anti-HER2 scFv-Fc(Ser396Sec)/CN29. The plasma concentrations of total antibody and intact ADC were quantified by ELISA at the indicated time points, using HER2 ECD for capturing and either anti-His mAb (total antibody) or anti-MMAF mAb (intact ADC) for detection. Shown are mean ± SD values for each time point. See also Figure S5, Figure S6, Figure S7, and Table S6.

    Journal: Cell chemical biology

    Article Title: Stable and potent selenomab-drug conjugates

    doi: 10.1016/j.chembiol.2017.02.012

    Figure Lengend Snippet: (A) Human breast cancer cell line KPL-4 was xenografted into the mammary fat pads of female NSG mice, grown to ~150 mm3, randomized into 5 groups comprising 6 mice each, and treated with i.v. (tail vein) injections of the indicated ADCs and controls four times every week at 5 mg/kg. Mean ± SD values are plotted. (B) Four female CD-1 mice were injected i.v. with 6 mg/kg of anti-HER2 scFv-Fc(Ser396Sec)/CN29. The plasma concentrations of total antibody and intact ADC were quantified by ELISA at the indicated time points, using HER2 ECD for capturing and either anti-His mAb (total antibody) or anti-MMAF mAb (intact ADC) for detection. Shown are mean ± SD values for each time point. See also Figure S5, Figure S6, Figure S7, and Table S6.

    Article Snippet: Human Lambda ELISA Quantitation Set , Bethyl Laboratories , Cat#E80-116.

    Techniques: Injection, Clinical Proteomics, Enzyme-linked Immunosorbent Assay

    KEY RESOURCES TABLE

    Journal: Cell chemical biology

    Article Title: Stable and potent selenomab-drug conjugates

    doi: 10.1016/j.chembiol.2017.02.012

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Human Lambda ELISA Quantitation Set , Bethyl Laboratories , Cat#E80-116.

    Techniques: Virus, Recombinant, Marker, Conjugation Assay, Proliferation Assay, Enzyme-linked Immunosorbent Assay, Quantitation Assay, Software