This Standard Reference Material (SRM) is intended for use as an analytical standard of known potassium (K) and chloride (Cl-) content. This lot of potassium chloride (KCl) was prepared to ensure a material of high purity and homogeneity and has been assayed after drying at 500 °C. A unit of SRM 999c consists of a single glass bottle containing 30 g of the material. This data is public in the Certificate of Analysis for this material.

Standard Reference Material-1721: Southern Oceanic Air. Ambient Nominal Amount of Substance Fraction for Carbon Dioxide, Methane & Nitrous Oxide. This Standard Reference Material (SRM) is a primary gas mixture for which the amount-of-substance fraction, expressed as concentration, may be related to secondary working standards. This SRM is intended for the calibration of instruments used for ambient carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) determinations and for other applications. This data is public in the Certificate of Analysis for this material.

This Standard Reference Material (SRM) is intended for use as an analytical standard of known purity. It is intended primarily for use in the calibration and standardization of procedures for potassium (K) and chloride (Cl-) determinations employed in clinical analysis, including those using ion-selective electrodes, and for routine critical evaluation of the daily working standards used in these procedures. This lot of potassium chloride (KCl) was prepared to ensure a material of high purity and homogeneity and has been assayed after heating at 110 degrees C to 120 degrees C.

The spreadsheet file reported herein provides centroid data, descriptive of deuterium uptake, for the Fab Fragment of NISTmAb (PDB: 5K8A) reference material, as measured by the bottom-up hydrogen-deuterium exchange mass spectrometry (HDX-MS) method. The protein sample was incubated in deuterium-rich solutions under uniform pH and salt concentrations between 3.6 degrees C and 25.4 degrees C for seven intervals ranging (0 to 14,400) s plus a control sample that simulates a Fab Fragment immersed for infinite time in D2O.

The NIST DART-MS Forensics Database is an evaluated collection of in-source collisionally-induced dissociation (is-CID) mass spectra of compounds of interest to the forensics community (e.g. seized drugs, cutting agents, etc.). The is-CID mass spectra were collected using Direct Analysis in Real-Time (DART) Mass Spectrometry (MS), either by NIST scientists or by contributing agencies noted per compound. The database is provided as a general-purpose structure data file (.SDF).

This database gives hydrogen-deuterium exchange mass spectrometry (HDX-MS) data from measurements of three purified IgG1 glycoform samples, predominantly G0F, G2F, and SAF, in isolation and in complexation with the high-affinity receptor, Fc(gamma)RIa (CD64). The IgG1 antibody used in this study, aIL8hFc, is a murine-human chimeric IgG1, which inhibits IL-8 binding to human neutrophils.

This data collection contains 5,228 infrared spectra of different compounds along with chemical structures for most of them. Spectra are provided on a CD-ROM in the JCAMP-DX (Joint Committee for Atomic and Molecular Physical Data 'Data Exchange') format. Chemical structures are provided in the MOL-file format. The IR data originated from two sources, from the so-called 'EPA Vapor-Phase IR Library' and from NIST laboratories.

The atomic weights are available for elements 1 through 118 and isotopic compositions or abundances are given when appropriate. Version 3.0.

This MEMS Calculator determines the following thin film properties from data taken with an optical interferometer or comparable instrument: a) residual strain from fixed-fixed beams, b) strain gradient from cantilevers, c) step heights or thicknesses from step-height test structures, and d) in-plane lengths or deflections. Then, residual stress and stress gradient calculations can be made after an optical vibrometer or comparable instrument is used to obtain Young's modulus from resonating cantilevers or fixed-fixed beams.

This resource consists of methods for matrix-assisted laser desorption ionization (MALDI) mass spectrometry on a wide variety of synthetic polymers. The methods are taken from the peer-review scientific literature. The database covers the period from 1988, the year of Tanaka's first paper on the subject, through 2011. Each recipe comes with a literature citation and associated digital object identifier (DOI) when available. The database currently contains entries for over 1250 polymer/matrix combinations.