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The
U-PLEX platform offers validated components that can be combined to create high quality assays quickly and easily.
U-PLEX Human Clusterin Assay has the essential components for an assay that measures Clusterin in a single-analyte format. For information on multiplexing Clusterin with other analytes, please see
U-PLEX Custom Biomarker Group 3 (human) Assays.
Related Key Terms:
molecular chaperone, cytoprotective, tissue injury, kidney injury
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Specifications
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Kit Contents
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Documentation
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References
Application(s)
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Metabolic
,
Kidney Injury
,
Toxicology
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Analyte(s)
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Clusterin
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Species
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Human
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Instrument(s)
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SECTOR Imager 2400
,
MESO QuickPlex SQ 120MM
,
MESO SECTOR S 600
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SECTOR Imager 6000
,
MESO SECTOR S 600MM
,
MESO QuickPlex SQ 120
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U-PLEX Group Compatibility
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Biomarker Group 3
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Plate Type
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96-well
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Capture Antibody
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Mouse Monoclonal
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Detection Antibody
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Goat Polyclonal
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LLOD (Sensitivity)
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57.7 pg/mL
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Dynamic Range
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57.7 - 500,000 pg/mL
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Sample Type
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Cell Culture Media, Plasma, Serum
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Usage Statement
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For Research Use Only. Not for use in diagnostic procedures.
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Storage Statement(s)
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Please refer to the product insert for the storage conditions of individual kit components.
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Storage Condition
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Multi-Component
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Gene ID(s)
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1191
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UniProt ID(s)
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P10909
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Schedule B Code
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3822.19.0000
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Product Description
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Storage
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Quantity per Kit
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2-8 °C
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1 each (1 plate size)
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2-8 °C
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1 vial (1 vial)
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2-8 °C
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1 each (1 plate)
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2-8 °C
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1 bottle (200 mL)
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≤-10 °C
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1 bottle (50 mL)
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≤-10 °C
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1 bottle (10 mL)
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RT
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1 bottle (18 mL)
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Product Description
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Storage
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Quantity per Kit
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2-8 °C
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1 each (5 plate size)
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2-8 °C
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5 vial (1 vial)
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2-8 °C
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5 each (1 plate)
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2-8 °C
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3 bottle (200 mL)
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≤-10 °C
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3 bottle (50 mL)
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≤-10 °C
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1 bottle (50 mL)
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RT
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1 bottle (90 mL)
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Product Description
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Storage
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Quantity per Kit
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2-8 °C
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5 each (5 plate size)
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2-8 °C
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25 vial (1 vial)
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2-8 °C
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25 each (1 plate)
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2-8 °C
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3 bottle (200 mL)
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2-8 °C
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2 bottle (1000 mL)
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≤-10 °C
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3 bottle (200 mL)
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≤-10 °C
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3 bottle (50 mL)
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RT
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5 bottle (90 mL)
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Product Inserts
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Datasheets
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Product Highlights
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SDS
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Title
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Journal
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Year
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Urinary biomarkers track the progression of nephropathy in hypertensive and obese rats.
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Assessment of cisplatin-induced kidney injury using an integrated rodent platform.
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Early prediction of polymyxin-induced nephrotoxicity with next generation urinary kidney injury biomarkers.
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Time course of renal proximal tubule injury, reversal, and related biomarker changes in rats following cisplatin administration.
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Renal biomarker changes associated with hyaline droplet nephropathy in rats are time and potentially compound dependent.
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