PIEZO1 Antibody

說明書

中文名稱：

PIEZO1兔多克隆抗體
貨號：

CSB-PA852881ESR1HU
規格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA852881ESR1HU at dilution of 1:100

Immunohistochemistry of paraffin-embedded human glioma using CSB-PA852881ESR1HU at dilution of 1:100
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) PIEZO1 Polyclonal antibody
Uniprot No.：

Q92508
基因名：

PIEZO1
別名：

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
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Piezo-type mechanosensitive ion channel component 1 protein (2230-2420AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

Non-conjugated
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

Antigen Affinity Purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
產品提供形式：

Liquid
應用范圍：

ELISA, IHC

推薦稀釋比：

Application	Recommended Dilution
IHC	1:20-1:200

Protocols：

ELISA Protocol
Immunohistochemistry (IHC) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

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.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

功能：

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.
基因功能參考文獻：
1. 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
2. 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
3. present study was designed to evaluate in hereditary xerocytosis the functional link between mutated Piezo1 and KCNN4 PMID: 28619848
4. the knockdown of PIEZO1 significantly reduced the cell-viability of SW982 cells. PMID: 29757938
5. analysis of Piezo1 domains by using localized force on magnetic nanoparticles PMID: 27694883
6. Piezo1-shRNA could inhibit the invasion of the osteosarcoma cells. PMID: 29065102
7. Piezo1 plays an important role in the apoptosis of human osteoarthritis-derived chondrocytes through a caspase-12-dependent pathway. PMID: 28731145
8. 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
9. The structural dynamics of the PIEZO1 channel activation and inactivation by coarse-grained modeling has been reported. PMID: 28905417
10. 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
11. 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
12. data demonstrate that PIEZO1 is required for the regulation of NO formation, vascular tone, and blood pressure. PMID: 27797339
13. The Piezo1 convert a variety of mechanical stimuli into channel activation and subsequent inactivation, and what molecules and mechanisms modulate Piezo function. PMID: 27743844
14. 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
15. 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
16. 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 mutation PMID: 26971963
17. 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
18. When the "split protein" is coexpressed, the parts associate to form a normal channel. PMID: 26963637
19. Mutations in PIEZO1 is associated with persistent lymphoedema caused by congenital lymphatic dysplasia. PMID: 26387913
20. 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
21. Mechanically activated Piezo1 plays an essential role in red blood cell volume homeostasis. PMID: 26001274
22. Piezo1 is amenable to chemical activation and thus there is a possibility that endogenous Piezo1 agonists might exist. PMID: 26001275
23. PIEZO1 is permeable to monovalent ions (K+, Na+, Cs+, Li+) and most divalent ions (Ba2+, Ca2+ and Mg2+), but not to Mn2+. PMID: 25955826
24. a possible role of Piezo1 in invasion and metastatic propagation. PMID: 25666479
25. Piezo1 channels are likely to function in normal RBCs and suggest a previously unidentified mechanotransductive pathway in ATP release. PMID: 26351678
26. study reports two unrelated families with hereditary xerocytosis where probands presented fetal hydrops for which the same heterozygous mutation in PIEZO1 was identified PMID: 23581886
27. PIEZO1 stretch sensitivity is modulated by polycystin-2. PMID: 24157948
28. family of mechanically activated channels that counts only two members in human, piezo1 and 2, has emerged recently. [review] PMID: 25037583
29. Protonation of the human PIEZO1 ion channel stabilizes inactivation. PMID: 25561736
30. 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
31. Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene have been found in a Danish pedigree. PMID: 24314002
32. The R2488Q PIEZO1 mutation is an apparent major cause of familial hereditary xerocytosis. PMID: 25044010
33. Piezo1 is a novel TFF1 binding protein that is important for TFF1-mediated cell migration in gastric cancer cells. PMID: 24798994
34. gating and inactivation as a function of pressure PMID: 23972840
35. 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
36. R2456H and R2488Q mutations in PIEZO1 alter mechanosensitive channel regulation, leading to increased cation transport in erythroid cells. PMID: 23479567
37. Xerocytosis is caused by mutations that alter the kinetics of the mechanosensitive channel PIEZO1. PMID: 23487776
38. 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
39. Loss of Fam38A expression may cause increased cell migration and metastasis in lung tumours. PMID: 22792288
40. Data show that the transmission of PIEZO1 mutations and cosegregation with the disease phenotype in all affected persons in both kindreds. PMID: 22529292
41. siRNA knockdown in epithelial cells inactivates endogenous beta1 integrin, reducing cell adhesion PMID: 20016066
42. The MIB index was strongly correlated with disease progression in papillary urothelial neoplasms in the urinary bladder. PMID: 18311491
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相關疾?。?/div>
Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema (DHS1); Lymphedema, hereditary, 3 (LMPH3)
亞細胞定位：

Endoplasmic reticulum membrane; Multi-pass membrane protein. Endoplasmic reticulum-Golgi intermediate compartment membrane. Cell membrane; Multi-pass membrane protein. Cell projection, lamellipodium membrane. Cell membrane; Multi-pass membrane protein.
蛋白家族：

PIEZO (TC 1.A.75) family
組織特異性：

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
數據庫鏈接：

HGNC: 28993

OMIM: 194380

KEGG: hsa:9780

STRING: 9606.ENSP00000301015

UniGene: Hs.377001

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