Rat Secondary Antibodies
Hach Company Application Software Enzymatic Food Analysis
The application software LZV937 is a compilation of enzymology testsmanufactured by R-Biopharm AG, Darmstadt that can be performed with the spectrophotometer DR 6000 and carousel insert LZV902.99.00001. The methods can be modified for individual settings.
Sigma Aldrich Fine Chemicals Biosciences MS RT Calibration Mix Prot
MSRT1 is an injection-ready standard and can serve for quick tests of LC-MS platform performance comparison of LC gradients and columns monitoring column and system changes. MSRT1 can be used to predict retention times of peptides across LC-MS platforms. MSRT1 is also applicable to multiple reaction monitoring / selected reaction monitoring (MRM / SRM) analysis. ComponentsEach vial contains various amounts of 14 isotopically labeled synthetic peptides dried via vacuum centrifugation. Each peptide is labeled with either a [13C6 15N2] Lysine (8 Da) a [13C6 15N4] Arginine (10 Da) or a [13C6 15N] Leucine (7 Da).
Cusabio Technology LLC Rat visfatin ELISA Kit
The Rat Visfatin ELISA Kit is designed for the quantitative detection of NAMPT (visfatin) in serum plasma and tissue homogenates using a sandwich assay format This kit detects NAMPT within a broad dynamic range of 3 12 ng/mL to 200 ng/mL with a high sensitivity of 0 78 ng/mL ensuring precise measurement of low-abundance samples The assay requires a short incubation time of 1-5 hours and a modest sample volume of 50-100 L per test Detection is performed at 450 nm providing reliable and reproducible results for research applications Its compatibility with multiple biological matrices makes it a versatile tool for studying NAMPT levels in metabolic and inflammatory research
Rockland Immunochemicals Fluorescent TrueBlot: Anti-Mouse Ig DyLight™ 800 - 18-4517-32
Fluorescent Mouse TrueBlot Antibody DyLight™ 800 may also be used for detection in immunoassays that do not employ IP. Provided as a lyophilized powder. We recommend incubating the blots from minigels in sealed bags with minimal volume (2-3 mLs). If used conservatively at 2.5mls/blot will yield enough reagent for 40 blots. Note that there are three key procedural considerations: 1. Protein A or G beads may be used with the mouse, goat and sheep TrueBlot secondaries, but not with the rabbit TrueBlot secondary. 2. Immunoprecipitate should be completely reduced. 3. BSA or MB-070 Blocking Buffer for Fluorescent WB, at low concentrations, should be used as the blocking protein for the WB. DO NOT USE BLOTTO or MILK. Note: To achieve best results when detecting mouse IgG1 subtypes, we recommend performing a dot blot or titration to determine the optimal dilution. Specific conditions for each protein and antibody combination should be specifically optimized by the end user.