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PE 22-28 (acetate)

(Synonyms: Gly-Val-Ser-Trp-Gly-Leu-Arg-OH) 目录号 : GC91810

PE 22-28 is a peptide inhibitor of the two-pore domain potassium channel K2P2.1/TREK1 (IC50 = 0.1 nM in HEK293 cells expressing the human channel) and a fragment of spadin .

PE 22-28 (acetate) Chemical Structure

规格 价格 库存 购买数量
500 µg
¥1,246.00
现货
1 mg
¥2,366.00
现货
5 mg
¥9,352.00
现货

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Sample solution is provided at 25 µL, 10mM.

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PE 22-28 is a peptide inhibitor of the two-pore domain potassium channel K2P2.1/TREK1 (IC50 = 0.1 nM in HEK293 cells expressing the human channel) and a fragment of spadin .[1] It is selective for K2P2.1/TREK1 over K2P10.1 /TREK2, K2P13.1/TRAAK, K2P18.1/TRESK, and K2P3.1/TASK1 in HEK293 cells expressing the human channels at 100 nM. PE 22-28 (4 µg/kg for four days) increases neurogenesis and the levels of postsynaptic density protein 95 (Psd-95), a measure of increased synaptogenesis, in isolated mouse hippocampi. It decreases immobility in the forced swim test, latency to feed in the novelty-suppressed feeding test, and the time to escape in the Porsolt learned helplessness test in mice when administered at a dose of 0.3 µg/kg for four days.

References:
[1].Djillani, A., Pietri, M., Moreno, S., et al.Shortened spadin analogs display better TREK-1 inhibition, in vivo stability and antidepressant activityFront. Pharmacol.8:643(2017).

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1 mg 5 mg 10 mg
1 mM 1.2922 mL 6.4608 mL 12.9216 mL
5 mM 0.2584 mL 1.2922 mL 2.5843 mL
10 mM 0.1292 mL 0.6461 mL 1.2922 mL
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