Scientific references

This page lists the numbers you look up at the bench. It has the periodic table, the SI prefixes, the units a lab writes on a bottle or a pipette, a few constants, the amino acids, the nucleotides, buffer pKa values at 25 °C, and the temperatures we set most often. The figures are reference values. If a mass or a pH has to be right, check the bottle and measure it yourself. The calculations are in the calculators.

Last updated: 24 October 2026

Periodic table

Pick an element. The molar mass is the one the molarity calculator uses. A number in brackets is the mass number of a long-lived isotope. Click an element to see the further details in the data block below.

SI prefixes

The prefixes a lab uses most.

SymbolNameFactor
Ttera10¹²
Ggiga10⁹
Mmega10⁶
kkilo10³
mmilli10⁻³
µmicro10⁻⁶
nnano10⁻⁹
ppico10⁻¹²
ffemto10⁻¹⁵

Units

The mark on the label, and what it counts. An ångström is not an SI unit. The same length is 0.1 nm. When a conversion and the label disagree, the figure on the bottle wins.

Length

SymbolNameWhat it counts
metreThe SI base unit of length. On the bench a length is usually a millimetre or a centimetre.
centimetreOne hundredth of a metre. Cuvettes, tubing and the size of a plate.
millimetreOne thousandth of a metre. The usual unit for glassware, tubing and an instrument bed.
micrometreOne thousandth of a millimetre. Filter pore size, particle size and the size of a cell.
nanometreOne thousandth of a micrometre. Wavelengths, nanoparticles and the finer pores of a membrane.
ångströmOne tenth of a nanometre, so 10⁻¹⁰ m, or 100 pm. Bond lengths, atomic and ionic radii, X-ray wavelengths and crystal lattice spacings. Not an SI unit. The SI name of the same length is 0.1 nm. Crystallography and older spectroscopy still print the ångström.
picometreOne hundredth of an ångström. Newer tables of ionic radii use the picometre.

Volume

SymbolNameWhat it counts
litreOne cubic decimetre. The catalogue also prints l for the same unit.
millilitreOne thousandth of a litre, and one cubic centimetre.
microlitreOne thousandth of a millilitre, and one cubic millimetre. The unit of a pipette. A label that prints uL means µl.
nanolitreOne thousandth of a microlitre. Some dispensers and droplet systems are quoted in nanolitres.

Mass

SymbolNameWhat it counts
kilogramA thousand grams. Balances and shipments.
gramThe usual mass on a reagent bottle.
milligramOne thousandth of a gram.
microgramOne thousandth of a milligram.
nanogramOne thousandth of a microgram. Immunoassays and standards.
picogramOne thousandth of a nanogram.
daltonThe same size as the unified atomic mass unit: 1 Da = 1 u. A molar mass of 180 g/mol is a molecular mass of 180 Da. The residue masses further down this page are in dalton.
kilodaltonA thousand dalton. The usual mass of a protein.

Amount and concentration

SymbolNameWhat it counts
moleThe SI unit of amount of substance. mmol, µmol, nmol and pmol are the steps of a thousand that a protocol actually writes.
molarOne mole per litre. 1 mM is 0.001 mol/L. 1 µM is 10⁻⁶ mol/L. 1 nM is 10⁻⁹ mol/L.
normalityEquivalents per litre, on older bottles. One normal is not always one molar. For sulphuric acid, 1 N is 0.5 mol/L. The bottle states which.
mass fractionGrams per 100 g of mixture.
mass per volumeGrams per 100 ml of solution.
volume per volumeMillilitres per 100 ml of solution.
parts per millionIn dilute water, 1 ppm is taken as 1 mg/L. That conversion does not hold for every matrix.
parts per billionIn dilute water, 1 ppb is taken as 1 µg/L.
enzyme unitOne micromole of substrate per minute, under the conditions named on the bottle. A unit of one enzyme is not a unit of another.
katalOne mole per second. 1 U is 16.67 nkat. Rare on a bottle. It is the SI unit of catalytic activity.
international unitDefined for that substance by a reference preparation. There is no universal size.
equivalentOne mole of reactive units, as the reaction defines them. Normality counts equivalents per litre.
osmolalityMilliosmoles per kilogram of solvent. Cell-culture media are often quoted in mOsm/kg.

Temperature and pressure

SymbolNameWhat it counts
degree CelsiusThe bench scale.
kelvin0 °C is 273.15 K. The degree is the same size.
pascalThe SI unit of pressure.
kilopascal1 kPa is 1000 Pa.
bar100 kPa, exactly 10⁵ Pa.
millibarOne thousandth of a bar, 100 Pa. Vacuum gauges and some autoclave charts.
atmosphereThe standard atmosphere, 101.325 kPa.
torr1/760 of a standard atmosphere. A bench gauge marked mmHg reads the same number for ordinary work.

Spin, light and water

SymbolNameWhat it counts
revolutions per minuteThe force depends on the rotor radius, so the number does not transfer to another rotor.
relative centrifugal forceMultiples of standard gravity. This is the number that transfers. With the radius r in centimetres and the speed n in revolutions per minute, × g = 1.118 × 10⁻⁵ × r × n².
svedberg10⁻¹³ seconds. Sedimentation, as in a 30S subunit.
absorbanceDimensionless. The log10 of the ratio of the intensities at a stated wavelength.
optical densityUsed as the absorbance at a named wavelength, for example OD600.
conductivityUltrapure water at 25 °C is 0.055 µS/cm.
resistivityThe same water is 18.2 MΩ·cm at 25 °C.
hertzOne cycle per second. A shaker is more often quoted in revolutions per minute.
second, minute, hourThe time on a protocol. s is the SI unit.

Molecules, counts and scales

SymbolNameWhat it counts
base pairA duplex is counted in base pairs. kb is 1000 bp. Mb is 10⁶ bp.
nucleotideA single strand is counted in nucleotides, a duplex in base pairs.
colony-forming unitA viable cell that forms one colony. Not a count under the microscope.
meshOpenings per inch. Not an SI length. The opening in micrometres depends on the wire. Compare sieves by the micrometre opening.
needle gaugeA scale, not a millimetre. A higher gauge is a thinner needle. The millimetre size is the one on the product.

From rpm to × g (relative centrifugal force)

A protocol should state the force, not the speed: rpm depends on the rotor radius, × g does not.

RCF = 1.118 × 10⁻⁵ × r × n², with r the rotor radius in centimetres (centre to the bottom of the tube, rmax) and n the speed in rpm. The other way round: n = √(RCF / (1.118 × 10⁻⁵ × r)).

Worked example. A rotor with r = 10 cm at 3 000 rpm: 1.118 × 10⁻⁵ × 10 × 3 000² = 1.118 × 10⁻⁵ × 10 × 9 000 000 ≈ 1 006 × g. A protocol that asks for 1 000 × g on a rotor with r = 8 cm needs n = √(1 000 / (1.118 × 10⁻⁵ × 8)) ≈ 3 344 rpm.

Constants at the bench

The SI values, rounded the way the bench uses them.

ConstantValue
NA6.022 × 10²³ mol⁻¹
R8.314 J·mol⁻¹·K⁻¹
F96 485 C·mol⁻¹
0 °C273.15 K
Vm22.4 L·mol⁻¹ at 0 °C and 101.325 kPa

Amino acids

Average residue mass in a protein chain, in dalton.

CodeResidue mass (Da)
AlaA71.08
ArgR156.19
AsnN114.10
AspD115.09
CysC103.14
GlnQ128.13
GluE129.12
GlyG57.05
HisH137.14
IleI113.16
LeuL113.16
LysK128.17
MetM131.19
PheF147.18
ProP97.12
SerS87.08
ThrT101.11
TrpW186.21
TyrY163.18
ValV99.13

Source: average residue masses calculated from the IUPAC standard atomic weights; they match the residue masses tabulated in the CRC Handbook of Chemistry and Physics (Properties of amino acids). Add 18.02 Da (one water) for the free peptide.

Nucleotides

Residue mass in a chain, in dalton.

BaseDNARNA
A313.2329.2
C289.2305.2
G329.2345.2
T / U304.2306.2

Source: calculated from the IUPAC standard atomic weights for the neutral nucleoside monophosphate minus one water, as used in common oligonucleotide mass tables.

Buffer pKa at 25 °C

The same pKa values as the buffer calculator. The useful window sits about one unit around the pKa.

BufferpKaUseful range
Tris8.077.1–9.1
HEPES7.566.8–8.2
MOPS7.206.5–7.9
Phosphate7.215.8–8.0
PIPES7.146.1–7.5
MES6.275.5–6.7
Acetate4.763.6–5.6

Sources: pKa values at 25 °C as tabulated in the CRC Handbook of Chemistry and Physics (Dissociation constants of organic acids and bases; Buffers for biological research) and in Goldberg, Kishore & Lennen, "Thermodynamic quantities for the ionization reactions of buffers", J. Phys. Chem. Ref. Data 31 (2002) 231 (NIST). PIPES: 7.14 at 25 °C per NIST (Goldberg et al. 2002). Published values differ by a few hundredths depending on ionic strength and method.

Molar extinction coefficients (UV, 280 nm)

The absorbance of a protein at 280 nm comes mainly from tryptophan, tyrosine and cystine (disulfide bonds).

Contributorε at 280 nm (M⁻¹·cm⁻¹)
Trp (W)5 500
Tyr (Y)1 490
Cystine125

Beer–Lambert law: A = ε × c × l, with A the absorbance, ε the molar extinction coefficient (M⁻¹·cm⁻¹), c the concentration (mol/L) and l the path length (cm). For a protein: ε280 = (nTrp × 5 500) + (nTyr × 1 490) + (ncystine × 125). Free cysteines do not count. The linear range of most photometers ends around A = 1 to 1.5.

Worked example. A 25 kDa protein with 2 Trp, 4 Tyr and 1 disulfide bond: ε = 2 × 5 500 + 4 × 1 490 + 125 = 17 085 M⁻¹·cm⁻¹. A measured A280 of 0.50 in a 1 cm cuvette gives c = 0.50 / 17 085 ≈ 2.93 × 10⁻⁵ M = 29.3 µM, or 29.3 µM × 25 000 g/mol ≈ 0.73 mg/mL.

Source: Pace, Vajdos, Fee, Grimsley & Gray, "How to measure and predict the molar absorption coefficient of a protein", Protein Science 4 (1995) 2411–2423.

Henderson–Hasselbalch equation

The ratio of base to acid that gives a buffer its pH.

pH = pKa + log10([A⁻] / [HA]), with [A⁻] the base form and [HA] the acid form. When both are equal, pH = pKa. It holds best within about one unit of the pKa and at moderate ionic strength.

Worked example. A 0.1 M phosphate buffer at pH 7.4 (pKa2 = 7.21): [HPO₄²⁻] / [H₂PO₄⁻] = 10^(7.4 − 7.21) = 10^0.19 ≈ 1.55. So [HPO₄²⁻] = 0.1 × 1.55 / 2.55 ≈ 0.061 M and [H₂PO₄⁻] ≈ 0.039 M. Check the pH with a calibrated meter and adjust; the buffer calculator does this arithmetic.

Dilution: C1V1 = C2V2

The amount of solute stays the same when you add solvent.

C1 × V1 = C2 × V2, with C1 the stock concentration, V1 the volume of stock, C2 the target concentration and V2 the final volume. Use the same units on both sides.

Worked example. 50 mL of 20 mM from a 1 M stock: V1 = (20 mM × 50 mL) / 1 000 mM = 1 mL. Pipette 1 mL of stock and make up to 50 mL, so add 49 mL of solvent. For large dilution factors, a serial dilution (for example two steps of 1:100 for 1:10 000) keeps pipetting error down. The dilution calculator does the same.

Temperatures at the bench

Usual set-points. Not a rule.

WhereTemperature
Ice bath0 °C
Room20–25 °C
Incubation, body37 °C
Heat shock42 °C
PCR, denaturation95 °C
PCR, extension72 °C
Autoclave121 °C
Freezer−20 °C
Ultra-low−80 °C
Liquid nitrogen−196 °C

Sources