DHS antibody; Fam38a antibody; Family with sequence similarity 38 member A antibody; KIAA0233 antibody; Membrane protein induced by beta-amyloid treatment antibody; Mib antibody; PIEZ1_HUMAN antibody; Piezo-type mechanosensitive ion channel component 1 antibody; PIEZO1 antibody; Protein FAM38A antibody; Protein FAM38B antibody; Protein PIEZO1 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Piezo-type mechanosensitive ion channel component 1 protein (2230-2420AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Pore-forming subunit of a mechanosensitive non-specific cation channel. Generates currents characterized by a linear current-voltage relationship that are sensitive to ruthenium red and gadolinium. Plays a key role in epithelial cell adhesion by maintaining integrin activation through R-Ras recruitment to the ER, most probably in its activated state, and subsequent stimulation of calpain signaling. In the kidney, may contribute to the detection of intraluminal pressure changes and to urine flow sensing. Acts as shear-stress sensor that promotes endothelial cell organization and alignment in the direction of blood flow through calpain activation. Plays a key role in blood vessel formation and vascular structure in both development and adult physiology. Acts as sensor of phosphatidylserine (PS) flipping at the plasma membrane and governs morphogenesis of muscle cells. In myoblasts, flippase-mediated PS enrichment at the inner leaflet of plasma membrane triggers channel activation and Ca2+ influx followed by Rho GTPases signal transduction, leading to assembly of cortical actomyosin fibers and myotube formation.
Gene References into Functions
Both vertebrate and invertebrate mechanosensitive PIEZO ion channels are polymodal, being voltage modulated, and can even be directly voltage gated following a preceding mechanical stimulus.PMID:29545531
In the absence of extracellular matrix (ECM) proteins Piezo1 receptors are relatively insensitive to mechanical forces pushing the cellular membrane, whereas they can hardly be activated by mechanically pulling the membrane. Yet, if conjugated with Matrigel, a mix of ECM proteins, the receptors become sensitized.PMID:28164706
present study was designed to evaluate in hereditary xerocytosis the functional link between mutated Piezo1 and KCNN4PMID:28619848
the knockdown of PIEZO1 significantly reduced the cell-viability of SW982 cells.PMID:29757938
analysis of Piezo1 domains by using localized force on magnetic nanoparticlesPMID:27694883
Piezo1-shRNA could inhibit the invasion of the osteosarcoma cells.PMID:29065102
Piezo1 plays an important role in the apoptosis of human osteoarthritis-derived chondrocytes through a caspase-12-dependent pathway.PMID:28731145
MiR-103a might be a potential biomarker of myocardium infarction and could be used as an index for the diagnosis of AMI. It may be involved in the development of HBP and onset of AMI through regulating the Piezo1 expression.PMID:27515482
The structural dynamics of the PIEZO1 channel activation and inactivation by coarse-grained modeling has been reported.PMID:28905417
Additional alterations in mutant PIEZO1 channel kinetics, differences in response to osmotic stress, and altered membrane protein trafficking, predicting variant alleles that worsen or ameliorate erythrocyte hydration.PMID:28716860
differential regulation of PKA and cell stiffness in unconfined versus confined cells is abrogated by dual, but not individual, inhibition of Piezo1 and myosin II.PMID:27160899
data demonstrate that PIEZO1 is required for the regulation of NO formation, vascular tone, and blood pressure.PMID:27797339
The Piezo1 convert a variety of mechanical stimuli into channel activation and subsequent inactivation, and what molecules and mechanisms modulate Piezo function.PMID:27743844
Because Piezo1 senses both mechanical crowding and stretch, it may act as a homeostatic sensor to control epithelial cell numbers, triggering extrusion and apoptosis in crowded regions and cell division in sparse regions.PMID:28199303
platelets and Meg-01 cells express the MS cation channel Piezo1, which may contribute to Ca(2+) entry and thrombus formation under arterial shear.PMID:28416610
correlation between HPCHA and PIEZO1-gene mutated findings raise an important question as to whether any of the high phosphatidylcholine hemolytic anemia cases previously diagnosed in Japan may have in fact been the form of hemolytic anemia known as hereditary xerocytosis or dehydrated hereditary stomatocytosis with PIEZO1 gene mutationPMID:26971963
Piezo1 responds to lateral membrane tension with exquisite sensitivity as compared to other mechanically activated channels and that resting tension can drive channel inactivation, thereby tuning overall mechanical sensitivity of Piezo1.PMID:26646186
When the "split protein" is coexpressed, the parts associate to form a normal channel.PMID:26963637
Mutations in PIEZO1 is associated with persistent lymphoedema caused by congenital lymphatic dysplasia.PMID:26387913
Homozygous and compound heterozygous mutations in PIEZO1, result in an autosomal recessive form of generalized lymphatic dysplasia with a high incidence of non-immune hydrops fetalis and childhood onset of facial and four limb lymphoedema.PMID:26333996
Mechanically activated Piezo1 plays an essential role in red blood cell volume homeostasis.PMID:26001274
Piezo1 is amenable to chemical activation and thus there is a possibility that endogenous Piezo1 agonists might exist.PMID:26001275
PIEZO1 is permeable to monovalent ions (K+, Na+, Cs+, Li+) and most divalent ions (Ba2+, Ca2+ and Mg2+), but not to Mn2+.PMID:25955826
a possible role of Piezo1 in invasion and metastatic propagation.PMID:25666479
Piezo1 channels are likely to function in normal RBCs and suggest a previously unidentified mechanotransductive pathway in ATP release.PMID:26351678
study reports two unrelated families with hereditary xerocytosis where probands presented fetal hydrops for which the same heterozygous mutation in PIEZO1 was identifiedPMID:23581886
PIEZO1 stretch sensitivity is modulated by polycystin-2.PMID:24157948
family of mechanically activated channels that counts only two members in human, piezo1 and 2, has emerged recently. [review]PMID:25037583
Protonation of the human PIEZO1 ion channel stabilizes inactivation.PMID:25561736
the mechanically gated ion channel Piezo1 is an important determinant of mechanosensitive lineage choice in neural stem cells and may play similar roles in other multipotent stem cells.PMID:25349416
Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene have been found in a Danish pedigree.PMID:24314002
The R2488Q PIEZO1 mutation is an apparent major cause of familial hereditary xerocytosis.PMID:25044010
Piezo1 is a novel TFF1 binding protein that is important for TFF1-mediated cell migration in gastric cancer cells.PMID:24798994
gating and inactivation as a function of pressurePMID:23972840
The gain-of-function PIEZO1 phenotype provides insight that helps to explain the increased permeability of cations in red blood cells of dehydrated hereditary stomatocytosis patients.PMID:23695678
R2456H and R2488Q mutations in PIEZO1 alter mechanosensitive channel regulation, leading to increased cation transport in erythroid cells.PMID:23479567
Xerocytosis is caused by mutations that alter the kinetics of the mechanosensitive channel PIEZO1.PMID:23487776
Piezo1 responses in a patch emulate many of the responses seen in whole-cell mode, there are significant differences, presumably in the force transfer structures.PMID:22790451
Loss of Fam38A expression may cause increased cell migration and metastasis in lung tumours.PMID:22792288
Data show that the transmission of PIEZO1 mutations and cosegregation with the disease phenotype in all affected persons in both kindreds.PMID:22529292
Expressed in numerous tissues. In normal brain, expressed exclusively in neurons, not in astrocytes. In Alzheimer disease brains, expressed in about half of the activated astrocytes located around classical senile plaques. In Parkinson disease substantia