NIST2925
Recombinant Human Serum Albumin Solution (Primary Reference Calibrator for Urine Albumin) (Frozen)
NIST®SRM®
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1 G
CHF 1’310.00
About This Item
UNSPSC-Code:
41116107
NACRES:
NA.24
Empfohlene Produkte
Form
liquid
Verpackung
pkg of 1 g (2 vials x 0.5mL each)
Hersteller/Markenname
NIST®
Methode(n)
mass spectrometry (MS): suitable
Anwendung(en)
clinical testing
Lagertemp.
−20°C
Allgemeine Beschreibung
Each unit of SRM 2925 consists of two vials, each containing approximately 0.5 mL of HSA in 50 mmol/L ammonium bicarbonate in water. For more information, please refer to the SDS and COA.
SRM 2925_cert
SRM 2925_SDS
SRM 2925_cert
SRM 2925_SDS
Anwendung
Recombinant human serum albumin (HSA) is a standard reference material (SRM) intended for calibration of liquid chromatography-tandem mass spectrometric procedures for the determination of albumin in urine.
Leistungsmerkmale und Vorteile
- NIST certified value for recombinant HSA was determined through amino acid analysis using (ID-LC-MS/MS) and is expressed as nanomoles per gram, and is metrologically traceable to the SI-derived units for molar concentration.
- Expiration of Certification, Instructions for handling, storage, and use are provided on the NIST certificate.
Sonstige Hinweise
- Details on expiration, storage, safety, usage, and source are provided in the NIST certificate.
- Notes on biomaterials, disposal, and transport are documented in SDS.
Please download a current certificate at nist.gov/SRM for current analytes and certified values.
Rechtliche Hinweise
NIST is a registered trademark of National Institute of Standards and Technology
SRM is a registered trademark of National Institute of Standards and Technology
Lagerklassenschlüssel
12 - Non Combustible Liquids
WGK
WGK 1
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Analysenzertifikate (COA)
Lot/Batch Number
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Jia Wang et al.
STAR protocols, 3(4), 101908-101908 (2023-01-04)
Here, we present a protocol to reprogram mouse and human fibroblasts into expandable cardiovascular progenitor cells (CPCs) via a defined small-molecule treatment. We describe steps to prepare fibroblasts and generate the chemically induced CPCs (ciCPCs), followed by expansion and differentiation
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