NIST967A
Creatinine in frozen human serum
NIST® SRM® 967a
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UNSPSC Code:
41116107
NACRES:
NA.24
Recommended Products
grade
certified reference material
Quality Level
form
liquid
packaging
pkg of set(4) (2 ea conc)
manufacturer/tradename
NIST®
technique(s)
mass spectrometry (MS): suitable
application(s)
clinical testing
format
matrix material
General description
This human blood serum creatinine is a standard reference material (SRM) that consists of four stoppered vials of frozen human serum, two vials each at two different creatinine concentration levels. Each vial contains 1.0 mL of human serum.
SRM 967A_cert
SRM 967A_SDS
SRM 967A_cert
SRM 967A_SDS
Application
This human blood serum creatinine is intended primarily for use in evaluating the accuracy of procedures for the determination of creatinine in human serum. It is also meant for use in validating working or secondary reference materials.
Other Notes
- For more information on storage, usage, and expiry refer to the NIST certificate.
- Notes for biomaterials, disposal, and transport information are available in SDS.
Certified for the analytes listed below.
Creatinine
See certificate for values and more details at nist.gov/SRM.
Creatinine
See certificate for values and more details at nist.gov/SRM.
Preparation Note
- The serum is shipped frozen on dry ice and, upon receipt, should be stored frozen until ready for use.
- Vials of the SRM to be analyzed should be removed from the freezer and allowed to stand at room temperature (20 °C to 25 °C) until thawed.
Legal Information
NIST is a registered trademark of National Institute of Standards and Technology
SRM is a registered trademark of National Institute of Standards and Technology
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
高风险级别生物产品--人源产品
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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W Greg Miller et al.
Advances in chronic kidney disease, 25(1), 7-13 (2018-03-04)
In 2002, the Kidney Disease Outcomes Quality Initiative guidelines for identifying and treating CKD recommended that clinical laboratories report estimated glomerular filtration rate (eGFR) with every creatinine result to assist clinical practitioners to identify people with early-stage CKD. At that
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