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PIEZO1 (基因名), Piezo-type mechanosensitive ion channel component 1 (蛋白名), PIEZ1_HUMAN.
产品名称:

Human PIEZO1/ Piezo-type mechanosensitive ion channel component 1 Peptide

货号:

SR3227h

监管等级:
商标:
EIAab®
种属:
Human
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Human PIEZO1 Peptide
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Human PIEZO1 Peptide
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R&D 技术数据
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[1].
"Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis."

[2].
"Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops."

[3].
"Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1."

[4].
"Xerocytosis is caused by mutations that alter the kinetics of the mechanosensitive channel PIEZO1."

[5].
"Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels."

[6].
"Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis."

[7].
"[Feeling the pressure? Identification of two proteins activated by mechanical forces]."

[8].
"The mechanosensitive ion channel Piezo1 is inhibited by the peptide GsMTx4."

[9].
"Piezo1 and Piezo2 are essential components of distinct mechanically activated cation channels."

[10].
"Mechanosensitive channels: in touch with Piezo."
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