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sheep genomic dna  (AMS Biotechnology)


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    AMS Biotechnology sheep genomic dna
    Sheep Genomic Dna, supplied by AMS Biotechnology, 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/product/sheep+genomic+dna/Sheep+Genomic+DNA%2C+Male/pmc06723549-98-7-10
    Average 96 stars, based on 1 article reviews
    sheep genomic dna - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    other:

    Article Title: Long-Term High-Altitude Hypoxia and Alpha Adrenoceptor-Dependent Pulmonary Arterial Contractions in Fetal and Adult Sheep
    Article Snippet: For each experiment, singly frozen sub-aliquots of sheep genomic DNA (Amsbio LLC) were used as a reference to estimate transcript copies per cell for each of the three α 1 -AR subtypes.

    Article Title: Long-Term High-Altitude Hypoxia and Alpha Adrenoceptor-Dependent Pulmonary Arterial Contractions in Fetal and Adult Sheep.
    Article Snippet: For each experiment, singly frozen sub-aliquots of sheep genomic DNA (Amsbio LLC) were used as a reference to estimate transcript copies per cell for each of the three α1-AR subtypes.



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    PCR amplification of bovine genomic DNA using internal primers designed from the ORF of buffalo RsaI sequences . Schematic representation (A) shows PCR strategy used for amplification of ORF regions of RsaI sequences corresponding to 489, 141, 112 and 135 bp, respectively (a-d) . Panel (B) shows PCR amplification of RsaI ORF regions and β-actin as control. The corresponding position of each PCR product is shown in Panel (A) . Sequence IDs are indicated on left, amplicons size on right and species are mentioned on top of the lanes.

    Journal: BMC Genomics

    Article Title: RsaI repetitive DNA in Buffalo Bubalus bubalis representing retrotransposons, conserved in bovids, are part of the functional genes

    doi: 10.1186/1471-2164-12-338

    Figure Lengend Snippet: PCR amplification of bovine genomic DNA using internal primers designed from the ORF of buffalo RsaI sequences . Schematic representation (A) shows PCR strategy used for amplification of ORF regions of RsaI sequences corresponding to 489, 141, 112 and 135 bp, respectively (a-d) . Panel (B) shows PCR amplification of RsaI ORF regions and β-actin as control. The corresponding position of each PCR product is shown in Panel (A) . Sequence IDs are indicated on left, amplicons size on right and species are mentioned on top of the lanes.

    Article Snippet: For Southern hybridization, approximately, 4-5 μg of buffalo, cattle, goat and sheep genomic DNA were subjected to restriction digestion using RsaI enzyme following supplier's (NEB) specifications.

    Techniques: Amplification, Sequencing