biotechnology

Layer 3 — Biology24 concepts in this subtree

Biotechnology — applied biology at the genetic-engineering / industrial-application grain. Foundations: (1) Polymerase Chain Reaction (PCR) exponential amplification (Mullis 1983, Saiki et al. 1985/1988): N(c) = N_0 · (1 + e)^c where N_0…

PCR exponential amplification: N(c) = N_0·(1+e)^c; e ∈ [0,1]
CRISPR-Cas9: sgRNA-directed DNA cleavage; 20-nt protospacer + 5'-NGG-3' PAM
Hardy-Weinberg: p² + 2pq + q² = (p+q)² = 1; F2 3:1 and 9:3:3:1
PCR at e=1, c=30: 2^30 = 1,073,741,824 ≈ 10^9-fold amplification
Hardy-Weinberg identity: p²+2pq+q² = (p+q)²; at p=q=1/2 → {1/4, 1/2, 1/4}
Mendel dihybrid: F2 ratio 9:3:3:1 sums to 16 = 2^4; fractions sum to 1
Monod chemostat kinetics: μ(S)=μ_max·S/(K_s+S); dS/dt, dX/dt ODE system with dilution D
Plasmid-loss exponential decay: fraction retained = e^{−λn}; binary-fission dilution Markov chain
CRISPR NHEJ indel yield: p_cut=1−e^{−μt}; Poisson-process per-cell-cycle cut-rate framework
Monod: S_ss=K_s·D/(μ_max−D); D_crit=μ_max·S_feed/(K_s+S_feed); at D=μ_max/4,K_s=S_feed: S_ss=S_feed/3
Plasmid-loss: f(n)=exp(−λn); n_half=log(2)/λ; at λ=ln2 → n_half=1; retained@2gen = 1/4
CRISPR indel: p_cut=1−e^{−μt}; t_half=log(2)/μ; at μt=1: p_cut=1−1/e; at μt=ln2: p_cut=1/2
mAb (Köhler-Milstein 1975)
rDNA (Cohen-Boyer 1973)
PCR (Mullis 1983)
CRISPR-Cas9 (2012)
Synthetic genome (Venter 2010)
Biomanufacturing scale-up
Recombinant DNA (Cohen-Boyer 1973)
Monoclonal Ab (Köhler-Milstein 1975)
CRISPR-Cas9 (Doudna-Charpentier 2012)
Phage display (Smith 1985)
Directed evolution (Arnold 1993)
CAR-T (Kymriah 2017)
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