TRPM3 Antibody, FITC conjugated
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中文名稱：TRPM3兔多克隆抗體, FITC偶聯
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貨號：CSB-PA884520LC01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) TRPM3 Polyclonal antibody
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Uniprot No.：
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基因名：TRPM3
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別名：TRPM3 antibody; KIAA1616 antibody; LTRPC3 antibody; Transient receptor potential cation channel subfamily M member 3 antibody; Long transient receptor potential channel 3 antibody; LTrpC-3 antibody; LTrpC3 antibody; Melastatin-2 antibody; MLSN2 antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human Transient receptor potential cation channel subfamily M member 3 protein (1606-1713AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：FITC
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：>95%, Protein G purified
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產品提供形式：Liquid
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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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.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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功能：Calcium channel mediating constitutive calcium ion entry. Its activity is increased by reduction in extracellular osmolarity, by store depletion and muscarinic receptor activation. In addition, forms heteromultimeric ion channels with TRPM1 which are permeable for calcium and zinc ions.
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基因功能參考文獻：
- this study shows that differential expression of TRPM3 and Ca2+ flux between NK cell subtypes may provide evidence for their role in the pathomechanism involving NK cell cytotoxicity activity in chronic fatigue syndrome/myalgic encephalomyelitis PMID: 27727448
- rs10780946 TRPM3 polymorphism is associated with asthma-exacerbated respiratory disease susceptibility. PMID: 26891941
- Phosphoinositols regulate TRPM3. PMID: 26517445
- Activation of TRPM3 channels increases the transcriptional activation potential of c-Fos in HEK293 cells. PMID: 26493679
- This is the first study to examine the involvement of TRPM channel gene variations on the risk of SSc incidence. Our results suggest roles of TRPM3 and TRPM5 gene variants in the susceptibility to or clinical expression of Systemic sclerosis PMID: 26546534
- The TRPM3 activity is rapidly and reversibly inhibited by activation of phosphatases. PMID: 26123194
- TRPM3 is a phosphoinositide-dependent ion channel. PMID: 26123195
- Missense mutation in the cation channel, TRPM3, underlies inherited cataract and glaucoma. PMID: 25090642
- TRPM3 channel activation changes the gene expression pattern of the cells by activating transcription of c-Jun-, ATF2-, and TCF-controlled genes. PMID: 25576487
- The von Hippel-Lindau tumor suppressor (VHL) represses TRPM3 directly through miR-204 and indirectly through another miR-204 target, Caveolin 1. PMID: 25517751
- Pregnenolone sulfate is a powerful activator of TRPM3-mediated gene transcription, while transcription is completely inhibited by mefenamic acid in cells expressing activated TRPM3 channels. PMID: 24895737
- Data using recombinant proteins expressed in vascular endothelial cells suggest that SigmaR1 (sigma 1-type opioid receptor) is not involved in regulation of calcium signaling via TRPC5/TRPM3 (transient receptor potential cation channels C5/M3). PMID: 23121507
- TRPM3-ICF deletion mutation variants are regulatory channel subunits fine-tuning TRPM3 channel activity. PMID: 22961981
- Progesterone (0.01-10muM) suppressed TRPM3 activity evoked by pregnenolone sulphate. PMID: 22000496
- Calmodulin and S100A1 protein interact with N terminus of TRPM3 channel. PMID: 22451665
- The inhibition of TRPM1 by zinc ions is primarily due to a short stretch of seven amino acids present only in the pore region of TRPM1 but not of TRPM3. PMID: 21278253
- Our data establish that TRPM3 channels constitute a regulated entry pathway for zinc ions in pancreatic beta-cells PMID: 20401728
- data suggest functional relevance of TRPM3 in contractile and proliferating phenotypes of vascular smooth muscle cells PMID: 20360246
- The hTRPM3 gene is comprised of 24 exons and maps to chromosome 9q-21.12 and is composed of 1555 amino acids with the characteristic six-transmembrane domain of TRPs and is expressed in kidney and, at lesser levels, in brain, testis, and spinal cord PMID: 12672827
- TRPM3 is the first ion channel activated by sphingolipids. PMID: 15550678
- the divalent cation selectivity of TRPM3 channels is regulated by altenrative splicing PMID: 15824111
- we give an overview of the identified TRPM3 variants and compare their functional properties--{REVIEW} PMID: 17217062
- TRPM3 did not reveal a otosclerosis-causing mutation PMID: 18224337
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亞細胞定位：Cell membrane; Multi-pass membrane protein.
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蛋白家族：Transient receptor (TC 1.A.4) family, LTrpC subfamily, TRPM3 sub-subfamily
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組織特異性：Expressed primarily in the kidney and, at lower levels, in brain, testis, ovary, pancreas and spinal cord. Expression in the brain and kidney was determined at protein level. In the kidney, expressed predominantly in the collecting tubular epithelium in t
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