The second, symbol $\mathrm{s}$, is the SI base unit of time. Its definition fixes the unperturbed frequency of the ground-state atomic transition between levels split by hyperfine structure in caesium with mass number $133$ to exactly $9192631770\mathrm{Hz}$. One second therefore corresponds to that many cycles of the specified electromagnetic radiation.^[ref]

A practical atomic clock realizes the reference by interrogating atoms and controlling a reference oscillation. Magnetic fields, motion and environmental effects require corrections: an exact unit definition does not make every physical realization free of measurement uncertainty.

A unit of area used for scattering cross-sections.

A unit of time equal to $86400$ seconds.

A trypsin colorimetric assay follows enzyme activity through absorbance at $405\mathrm{nm}$. Trypsin cleaves an amide bond in the synthetic arginine derivative BAPNA, releasing p-Nitroaniline.^[ref]

The inspected Sigma procedure prepares fresh trypsin in cold $1\mathrm{mM}$ hydrochloric acid and fully dissolves $1mg/ml$ BAPNA. Its buffer solution stock contains $200\mathrm{mM}$ triethanolamine and $20\mathrm{mM}$ calcium chloride, at pH $7.8$. Three $3.00\mathrm{ml}$ cuvettes compare trypsin, trypsin plus the enzyme inhibitor aprotinin, and a blank replacing trypsin with its acid solvent. Sodium chloride solution replaces aprotinin in the uninhibited control. A thermostatted instrument for spectrophotometry holds $25{}^{\circ }\mathrm{C}$ and a $1\mathrm{cm}$ light path. After equilibration, adding BAPNA starts approximately five minutes of absorbance recording. The uninhibited sample checks activity; the blank checks background; the inhibited sample tests suppression.^[ref]

Let $s_U$, $s_I$ and $s_B$ denote the measured absorbance slopes per minute over the same linear time interval. Blank subtraction gives $s_U-s_B$ and $s_I-s_B$. If p-Nitroaniline accounts for the changing absorbance, the Beer-Lambert law givesHere $c$ is product molar concentration and $l$ is the geometric light path through the chemical solution. Sigma uses $\epsilon =9.96\mathrm{m}{\mathrm{M}}^{-1}\mathrm{c}{\mathrm{m}}^{-1}$.^[ref]

Choose original illustrative slopes $s_U=0.1036$, $s_I=0.0538$ and $s_B=0.0040\mathrm{mi}{\mathrm{n}}^{-1}$. The corrected uninhibited slope is $0.0996\mathrm{mi}{\mathrm{n}}^{-1}$, giving $dc/dt=0.0100\mathrm{mM}\mathrm{mi}{\mathrm{n}}^{-1}=10.0\mu \mathrm{M}\mathrm{mi}{\mathrm{n}}^{-1}$ at $l=1\mathrm{cm}$. In $3.00\mathrm{ml}$, the product amount of substance increases at $0.0300\mu \mathrm{mol}\mathrm{mi}{\mathrm{n}}^{-1}$. The corrected inhibited slope is $0.0498\mathrm{mi}{\mathrm{n}}^{-1}$, half as large. The relative suppression is thereforeThe background cancels in the numerator, but remains essential in the denominator. Using uncorrected slopes would instead give about $48.07\%$. Differentiating $A_{405}=\epsilon lc$ with fixed $\epsilon$ and $l$ explains the rate conversion; dimensional analysis checks it independently, since $\mathrm{mi}{\mathrm{n}}^{-1}/(\mathrm{m}{\mathrm{M}}^{-1}\mathrm{c}{\mathrm{m}}^{-1}\mathrm{cm})=\mathrm{mM}\mathrm{mi}{\mathrm{n}}^{-1}$.

The inference is a reaction rate on BAPNA under the stated conditions, rather than a direct count of trypsin molecules or proof of every cut in a protein. Cloudiness, other absorbing solutes, or different product protonation can compromise the Beer-Lambert law interpretation. A matched blank and a linear interval are therefore part of the measurement's meaning. A coloured enzyme inhibitor may require its own matched blank; a changed substrate or pH requires a fresh calibration. The constructed constant slopes above describe only that interval, not indefinite product accumulation.

Write a peptide's protein primary structure from its N-terminus toward its C-terminus. The usual simplified trypsin cleavage specificity rule places a cut immediately after K (lysine) or R (arginine), unless the next amino acid residue is P (proline). The following amino acid residue is essential: a terminal K or R has no following peptide bond to cut. The inspected institutional documentation describes proline as usually blocking cleavage, and explicitly lists sequence contexts in which that blocking is negligible. It also warns that experimental results can differ from sequence-based predictions. Thus “never before proline” is too strong.^[ref]

For an original worked example, stipulate complete cleavage at all sites allowed by that simplified rule in the twelve-amino acid residue sequenceA denotes alanine, G denotes glycine, and K, R and P have the meanings above. Cuts follow positions $3$, $7$ and $10$. Position $5$ is R, but its following P suppresses that cut in the stipulated rule; position $12$ is terminal K. Notice that the R in ARPK is retained inside the fragment, despite being a usually favoured trypsin target.

Near neutral pH, the lysine and arginine amino acid side chains undergo predominant protonation and carry positive electric charge. This helps distinguish those amino acid residues from the uncharged letter symbols used to write the sequence; those symbols specify identities, not whole-fragment electric charges.^[ref]

Fragment accounting checks the prediction: lengths $3+4+3+2=12$ conserve the twelve amino acid residues. The original linear chain has eleven peptide bonds; the four fragments retain $2+3+2+1=8$, so three were hydrolysed. Three water molecules are consumed per original chain in this formal stoichiometry. More generally, cutting $m$ distinct bonds of one linear peptide makes $m+1$ fragments: each cut splits one connected piece into two. This argument assumes an unbranched chain without additional links joining the pieces.

A missed trypsin cleavage at position $7$ would instead give $\mathrm{AGK}|\mathrm{ARPKAGR}|\mathrm{AK}$, merging two neighbouring fragments without changing their order. Even a correct cleavage preference does not guarantee complete proteolysis; predicted fragment boundaries describe a model, while actual boundaries require evidence from the digest.

Cited passages: physicist’s career and life years; Hahn and Strassmann’s chemical findings and Meitner and Frisch’s physical interpretation; author byline and book-provenance footer.

Missing transverse momentum is the negative vector sum of reconstructed visible transverse momenta, with detector corrections specified. Under the ideal hypotheses of zero total incoming transverse momentum, complete visible reconstruction and exactly one invisible neutrino, momentum conservation givesThe neutrino is not directly seen. Even under these ideal hypotheses, its longitudinal momentum $p_{z\nu }$ is not measured. Beam remnants can carry substantial unobserved longitudinal momentum; the colliding quarks' longitudinal momenta are also unknown event by event. Imposing an assumed parent mass can constrain $p_{z\nu }$, but that imports a hypothesis rather than measuring it. Finite coverage, poorly reconstructed particle jets and other invisible particles can also generate or modify missing transverse momentum.

An original teaching model exposes the roles of input loading, output loading and the supply. Choose a small-signal model with positive input electrical resistance $r_i$, transconductance $g_m>0$, and output electrical resistance $r_o>0$. Its controlled output current source draws $g_m{v}_i$ from the output node toward the reference node. This chosen sign gives an inverting voltage gain; it is not the historical contact circuit's sign convention.

Assume a fixed operating point, negligible reverse coupling, a frequency range where coupling capacitors pass the signal, and negligible other capacitances and transit delays. A collector resistor $R_D$ connects the output to a steady ideal supply $V_{DD}$; an external electrical load $R_L$ is coupled through a capacitor, so it draws no direct current. The input source has series electrical resistance $R_s$. All voltages below are small departures from the operating point. An ideal fixed supply has zero incremental voltage and therefore becomes the reference node in the small-signal model.

Define $R_O=R_D\parallel r_o$ and $R_P=R_O\parallel R_L$, where $a\parallel b=ab/(a+b)$. Input voltage division and output Kirchhoff's current law giveConsequently the port voltage gain, overall source-to-output voltage gain, and load current gain magnitudes areThis current gain uses load electric current, not all the controlled-source electric current. It is also a different port definition from the historical emitter-to-collector current gain. Larger $R_s$ attenuates the input; smaller $R_L$ attenuates the output.

For a sinusoid input signal, use root mean square voltages. The power gain from accepted input signal power $P_i=v_i^2/r_i$ to useful load power $P_L=v_o^2/R_L$ isUnlike $|A_i|$, this tends to zero as either $R_L\to 0$ or $R_L\to \infty$. Differentiation givesThus matching the output electrical load maximizes delivered power in this unilateral resistive model. For fixed source voltage, input loading multiplies $P_L$ by $[r_i/(R_s+r_i){]}^2$; the accepted-input power gain above excludes the loss in $R_s$.

Choose $r_i=R_s=1\mathrm{k\Omega }$, $g_m=2\mathrm{mS}$, $r_o=20\mathrm{k\Omega }$, and $R_D=2\mathrm{k\Omega }$. Then $R_O=20/11\mathrm{k\Omega }$. With $R_L=2\mathrm{k\Omega }$ and $v_s=20\mathrm{mV}$ root mean square, the input is $10\mathrm{mV}$ and the inverted output has magnitude $19.0476\mathrm{mV}$ root mean square. Hence $P_i=0.100\mu \mathrm{W}$ and $P_L=0.181406\mu \mathrm{W}$: $G_P=1.81406$. These are calculated values of the chosen model, not historical measurements.

With the same parameters but $R_L=100\Omega$, $|A_i|=1.89573$ while $G_P=0.359381<1$. At $R_L=10\mathrm{k\Omega }$, $|A_v|=3.07692$ while $G_P=0.946746<1$. Neither current gain nor voltage gain alone establishes power gain.

For the direct current load line in the figure, choose $V_{DD}=6\mathrm{V}$, $I_Q=1\mathrm{mA}$ and $V_Q=4\mathrm{V}$, consistent with $V_Q=V_{DD}-R_D{I}_Q$. Locally extend the model as $I=I_Q+g_m{v}_i+(V-V_Q)/r_o$. With the external electrical load isolated at direct current, its intersection with $I=(V_{DD}-V)/R_D$ is $V=V_Q-g_m{R}_O{v}_i$. Keeping $|v_o|$ small compared with the available voltage headroom is essential; extrapolation to arbitrarily large signals would be unphysical.

At the chosen operating point the collector supply delivers $V_{DD}{I}_Q=6\mathrm{mW}$: $2\mathrm{mW}$ is dissipated in $R_D$ and $4\mathrm{mW}$ in the output device. Under a small signal, that energy flow is redistributed to provide load power. The incremental controlled current source hides the supply's steady energy flow; it does not create energy. A real complete amplifier also needs its input biasing network and has further losses. This calculation establishes neither its total efficiency nor a universal law for point-contact transistors.

A bipolar junction transistor has two p-n junctions sharing a thin base region, arranged n-p-n or p-n-p. In its forward amplification regime, the emitter junction injects minority carriers; many cross the base before electron-hole recombination and reach the reverse-biased collector junction.^[ref]

A point-contact transistor has two closely spaced rectifying contacts, the emitter and collector, and a third low-electrical resistance base contact to the semiconductor. The Bardeen-Brattain point-contact transistor experiment established amplification using this arrangement. It does not require two fabricated bulk p-n junctions.

A transistor whose gate controls an electric field that changes conduction through a channel between source and drain. Changing the gate's electric potential difference controls the channel electric current.