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Merck
CN

NIST967A

Creatinine in frozen human serum

NIST® SRM® 967a

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NACRES:
NA.24
UNSPSC Code:
41116107
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grade

certified reference material

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

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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

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.

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.

Other Notes

Certified for the analytes listed below.
Creatinine

See certificate for values and more details at nist.gov/SRM.
  • For more information on storage, usage, and expiry refer to the NIST certificate.
  • Notes for biomaterials, disposal, and transport information are available in SDS.

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

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

高风险级别生物产品--人源产品
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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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