lambda fixii vector (Agilent technologies)
90
Structured Review
Agilent technologies
lambda fixii vector
Lambda Fixii Vector, 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/lambda+fixii/pmc01779807-439-21-24
Average 90 stars, based on 1 article reviews
Lambda Fixii Vector, 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/lambda+fixii/pmc01779807-439-21-24
Average 90 stars, based on 1 article reviews
lambda fixii vector - by Bioz Stars,
2026-10
90/100 stars
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Cloning:Article Title: Use of polynucleotides encoding small acid-soluble spore protein for inhibiting bacterial cell growth and/or treating bacterial infections Article Snippet: .. There are two classes of lambda cloning vectors: insertion vectors accept 0-12 kb DNA and include Lambda ZAPII, Uni-ZAP XR, and Lambda ZAP-Express (Stratagene); replacement vectors accept 9-23 kb and include Article Title: Use of polynucleotides encoding small acid-soluble spore protein for inhibiting bacterial cell growth and/or treating bacterial infections Article Snippet: .. There are two classes of lambda cloning vectors: insertion vectors accept 0-12 kb DNA and include Lambda ZAPII, Uni-ZAP XR, and Lambda ZAP-Express (Stratagene); replacement vectors accept 9-23 kb and include BAC Assay:Article Title: The family of DOF transcription factors: from green unicellular algae to vascular plants. Article Snippet: .. Screening of barley genomic, BAC and EST libraries A 150 bp probe corresponding to the DOF domain of the barley Pbf gene (Mena et al. 1998) was used to screen a Hordeum vulgare cv Morex BAC library and a cv Igri genomic library in Construct:Article Title: The barley cystatin gene (Icy) is regulated by DOF transcription factors in aleurone cells upon germination. Article Snippet: .. Igri genomic library constructed in Derivative Assay:Article Title: The barley cystatin gene (Icy) is regulated by DOF transcription factors in aleurone cells upon germination. Article Snippet: .. Igri genomic library constructed in Polymerase Chain Reaction:Article Title: Purification, cloning, and properties of alpha-galactosidase from Saccharopolyspora erythraea and its use as a reporter system. Article Snippet: An α-galactosidase from the erythromycinproducing bacterium Saccharopolyspora erythraea was purified to near homogeneity.. The enzyme has an apparent molecular mass of 45 kDa as determined by SDS-PAGE.. The pH optimum, Km for p-nitrophenyl-α-D-glucopyranoside (pNPαG), Km for melibiose and the Vmax are similar to those of other studied α-galactosidase enzymes. Purification:Article Title: Purification, cloning, and properties of alpha-galactosidase from Saccharopolyspora erythraea and its use as a reporter system. Article Snippet: An α-galactosidase from the erythromycinproducing bacterium Saccharopolyspora erythraea was purified to near homogeneity.. The enzyme has an apparent molecular mass of 45 kDa as determined by SDS-PAGE.. The pH optimum, Km for p-nitrophenyl-α-D-glucopyranoside (pNPαG), Km for melibiose and the Vmax are similar to those of other studied α-galactosidase enzymes. Labeling:Article Title: Purification, cloning, and properties of alpha-galactosidase from Saccharopolyspora erythraea and its use as a reporter system. Article Snippet: An α-galactosidase from the erythromycinproducing bacterium Saccharopolyspora erythraea was purified to near homogeneity.. The enzyme has an apparent molecular mass of 45 kDa as determined by SDS-PAGE.. The pH optimum, Km for p-nitrophenyl-α-D-glucopyranoside (pNPαG), Km for melibiose and the Vmax are similar to those of other studied α-galactosidase enzymes. Hybridization:Article Title: Purification, cloning, and properties of alpha-galactosidase from Saccharopolyspora erythraea and its use as a reporter system. Article Snippet: An α-galactosidase from the erythromycinproducing bacterium Saccharopolyspora erythraea was purified to near homogeneity.. The enzyme has an apparent molecular mass of 45 kDa as determined by SDS-PAGE.. The pH optimum, Km for p-nitrophenyl-α-D-glucopyranoside (pNPαG), Km for melibiose and the Vmax are similar to those of other studied α-galactosidase enzymes. |