5'-DMT-dC(Bz)-Suc-CPG; 1000 Å

Catalog number: BRP-02271

5'-DMT-dC(Bz)-Suc-CPG; 1000 Å

5'-DMT-dC(Bz)-Suc-CPG is used to add unmodified dC to the 3' end of the oligonucleotide.

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.
Catalog
BRP-02271
Synonyms
5'-O-DMT-2'-deoxy-C(Bz)-3'-O-Suc-CPG; 1000 Å
Appearance
White powder
Storage
Store at 2-8 °C
Shipping
Room temperature.
Cleavage Conditions
Cleave in concentrated ammonia for 90 minutes at 25°C.
Deprotection Conditions
Deprotect in concentrated ammonia for 5 hours at 60°C.

Chemical Structure:

Reference Reading

1. Liquid Marble Photosensor
Andrew Adamatzky, Michail-Antisthenis Tsompanas, Thomas C Draper, Claire Fullarton, Richard Mayne. Chemphyschem. 2020 Jan 3;21(1):90-98. doi: 10.1002/cphc.201900949.
A liquid marble is a liquid droplet coated by a hydrophobic powder. The liquid marble does not wet adjacent surfaces and therefore can be manipulated as a dry soft body. A Belousov-Zhabotinsky (BZ) reaction is an oscillatory chemical reaction exhibiting waves of oxidation. We demonstrate how to make a photo-sensor from BZ medium liquid marbles. We insert electrodes into a liquid marble, prepared from BZ solution and coated with polyethylene powder. The electrodes record a potential difference which oscillates due to oxidation wave-fronts crossing the electrodes. When the BZ marble is illuminated by a light source, the oxidation wave-fronts are hindered and, thus, the electrical potential recorded ceases to oscillate. We characterise several types of responses of BZ marble photosensors to various stimuli, and provide explanations of the recorded activity. BZ liquid marble photosensors may find applications in the fields of liquid electronics, soft robotics and unconventional computing.
2. Border-zone and watershed infarctions
Cataldo D'Amore, Maurizio Paciaroni. Front Neurol Neurosci. 2012;30:181-4. doi: 10.1159/000333638.
Border-zone (BZ) and watershed infarcts occur at the junction of two artery territories and are precipitated by a hemodynamic impairment although they cannot be excluded from microembolic etiology. These strokes may often be preceded by specifically precipitating circumstances that induce hypotension and/or hypovolemia (rising from a supine position, exercise, Valsalva's maneuver, administration of antihypertensive drugs, bleeding and anemia). Anterior BZ infarction occurs with a motor deficit of one or both contralateral limbs, associated with aphasia or mood disturbance. Campimetric disturbances are a constant feature of posterior BZ infarct associated with fluent aphasia and hemihypoesthesia. Subcortical and capsule-thalamic BZ infarctions often mimic lacunar syndrome due to small-vessel disease. Cerebellar BZ infarction is associated with non-specific vertigo syndrome or ataxia, while in brainstem BZ infarction patients are comatose with other signs of brainstem being compromised.
3. 3-Quinuclidinyl benzilate (agent BZ) toxicokinetics in rats
Alzbeta Dlabkova, David Herman, Lenka Cechova, Milos Hroch, Nela Vanova, Jana Zdarova Karasova. Basic Clin Pharmacol Toxicol. 2021 Sep;129(3):246-255. doi: 10.1111/bcpt.13627.
3-Quinuclidinyl benzilate (BZ) ranks among incapacitating military warfare agents. It acts as a competitive inhibitor on muscarinic receptors leading to non-lethal mental impairment. The present study aimed to investigate toxicokinetics of BZ in rats. Moreover, BZ can be exploited to produce a pharmacological model of Alzheimer's disease; thus, this paper focuses mainly on the BZ distribution to the brain. Wistar rats were administered i.p. with BZ (2 and 10 mg/kg). The BZ concentration was determined using LC-MS/MS in plasma, urine, bile, brain, kidney and liver. The sample preparation was based on a solid phase extraction (liquids) or protein precipitation (organ homogenates). The plasma concentration peaked at 3 min (204.5 ± 55.4 and 2185.5 ± 465.4 ng/ml). The maximal concentration in the brain was reached several minutes later. Plasma elimination half-life was 67.9 ± 3.4 in the 2 mg/kg group and 96.6 ± 27.9 in the 10 mg/kg group. BZ concentrations remained steady in the brain, with slow elimination (t1/2 506.9 ± 359.5 min). Agent BZ is excreted mainly via the urine. Steady BZ concentration in the brain could explain the previously published duration of the significant impairment in passive avoidance tasks in rats after an injection of BZ.
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