RAB1762
Human Troponin I ELISA
for serum, plasma and cell culture supernatants
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About This Item
UNSPSC Code:
41116158
NACRES:
NA.32
CA$138.00
Please contact Customer Service for Availability
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species reactivity
human
packaging
kit of 96 wells (12 strips x 8 wells)
technique(s)
ELISA: suitable
input
sample type serum
sample type cell culture supernatant(s)
sample type plasma
assay range
inter-assay cv: <12%
intra-assay cv: <10%
sensitivity: 0.61 ng/mL
standard curve range: 0.614-150 ng/mL
detection method
colorimetric
shipped in
wet ice
storage temp.
−20°C
Gene Information
human ... TNNI2(7136)
General description
This ELISA antibody pair detects Human Troponin I Type 2 (Skeletal, Fast) (TNNI2)
Application
For research use only. Not for use in diagnostic procedures.
Please refer to the attached Protocolfor details.
Please refer to the attached Protocolfor details.
Other Notes
A sample Certificate of Analysis is available for this product. Please type the word sample in the text box provided for lot number.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Met. Corr. 1
Storage Class Code
8A - Combustible corrosive hazardous materials
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Karl J Bonney et al.
The Journal of organic chemistry, 76(1), 97-104 (2010-12-01)
9-Oxabicyclo[6.1.0]non-4-ene (1) undergoes intramolecular bromonium ion-assisted epoxide ring-opening using N-bromosuccinimide via a presumed oxonium ion that is subject to stereospecific, nonregioselective capture with added external nucleophiles producing novel bicyclo[4.2.1] and bicyclo[3.3.1] ethers. Carboxylic acids (as catalyzed by tetramethylguanidine), alcohols, water
Stereoselective synthesis of cyclic ethers via bromine assistedepoxide ring expansion.
Davies SG, et al.
Tetrahedron Letters, 26(11), 1461-1464 (1985)
Transannular oxygen participation in halofluorination reactions of 9-oxabicyclo [6.1. 0] non-4-ene [1].
Haufe G, et al.
Journal of Fluorine Chemistry, 46(1), 83-95 (1990)
High-yielding, two-step 18F labeling strategy for 18F-PARP1 inhibitors.
Edmund J Keliher et al.
ChemMedChem, 6(3), 424-427 (2011-03-02)
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