TPI1 Antibody, Biotin conjugated

說明書

中文名稱：

TPI1兔多克隆抗體, Biotin偶聯
貨號：

CSB-PA13499D0Rb
規格：

￥880
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) TPI1 Polyclonal antibody
Uniprot No.：

P60174
基因名：

TPI1
別名：

TPI1 antibody; TPI antibody; Triosephosphate isomerase antibody; TIM antibody; EC 5.3.1.1 antibody; Methylglyoxal synthase antibody; EC 4.2.3.3 antibody; Triose-phosphate isomerase antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Triosephosphate isomerase protein (169-228AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

Biotin
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
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
應用范圍：

ELISA
Protocols：

ELISA 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：

Triosephosphate isomerase is an extremely efficient metabolic enzyme that catalyzes the interconversion between dihydroxyacetone phosphate (DHAP) and D-glyceraldehyde-3-phosphate (G3P) in glycolysis and gluconeogenesis.; It is also responsible for the non-negligible production of methylglyoxal a reactive cytotoxic side-product that modifies and can alter proteins, DNA and lipids.
基因功能參考文獻：
1. Disease-associated variants change well-conserved residues in the protein's sequence and affect protein stability. PMID: 28341520
2. A guide to the effects of a large portion of the residues of triosephosphate isomerase on catalysis, stability, druggability, and human disease has been presented. (Review) PMID: 28378917
3. Results revealed that TPI expression might be considered as a novel prognostic factor to evaluate gastric cancer patients' survival PMID: 28489783
4. TPI1 functions as a tumor suppressor in hepatocellular carcinoma and might serve as a potential therapeutic target for the treatment of HCC PMID: 27908734
5. our findings are the first to identify, to our knowledge, a functional synaptic defect in TPI deficiency derived from molecular changes in the TPI dimer interface. PMID: 27031109
6. Polyvinylpyrrolidone stabilised silver nanoparticles (60 nM; 2-6 nm diameter) selectively inhibited PfTIM with a 7-fold decrease in enzyme catalytic efficiency (K(cat)/K(m)) over hTIM. PMID: 26353595
7. results suggest amyloid-beta oligomers induce neuronal death by triggering methylglyoxal(MG) production; increased release of MG is a direct consequence of triosephosphate isomerase nitrotyrosination due to amyloid-beta peptide action at the 2 tyrosines associated with the catalytic center PMID: 24614897
8. TPI-PEP co-crystal structure, demonstrating that PEP directly binds into the catalytic pocket of TPI. PMID: 24598263
9. E104D mutant is highly susceptible to proteolysis, which in all likelihood contributes to the pathogenesis of enzymopathy. In addition, the proteolysis data on wild type HsTIM illustrate an asymmetric conduct of the two monomers. PMID: 24056040
10. Data suggest that exchange reactions during gluconeogenesis catalyzed by triose-phosphate isomerase and transaldolase do not differ between subjects with type 2 diabetes and control subjects under fasting or hyperglycemic conditions. PMID: 23736541
11. we review the relationship between modified TPI and Alzheimer disease (AD), highlighting the relevance of this protein in AD pathology PMID: 23233058
12. study found promoter SNPs of CKB and TPI1 were weakly associated with schizophrenia;in addition, IFNG polymorphisms were associated with schizophrenia; results suggest that IFNG and proteins affected by IFNG may play a role in the pathogenesis of schizophrenia PMID: 22623148
13. [Review] The activity of glycolytic enzyme TPI reveals a mechanistic link between energy metabolism and age-related proteostatic dysfunction which can suppress generation of altered proteins that characterize the aged phenotype in cells and tissues. PMID: 21651995
14. A patient with triosephosphate isomerase-deficiency was found to be homozygous for a Val231Met mutation. PMID: 21215915
15. A proteomic approach for identification and localization of the pericellular components of chondrocytes. PMID: 21698479
16. structural changes rather than abnormal catalysis may play an important role in the clinical manifestations of TPI deficiency; the postulated high aggregation ability of the unstable Glu104Asp mutant would lead to more serious symptoms PMID: 20546019
17. TPI1 were up-regulated with the malignancy of prostate cancer cell lines and have their potential as serum biomarkers for indicating the developmental stage of prostate cancer. PMID: 20233700
18. of two previously undescribed mutations: c.722 T>C (Phe240Ser) and c.28 insG; each of the two unrelated patients showed the new mutation in compound heterozygosity with the most common variant Glu104Asp, resulting in a very severe clinical pattern. PMID: 20374271
19. the dimerization behavior of TPI is influenced by the particular mutations investigated, and by the use of a potential alternative translation initiation site in the TPI gene PMID: 17183658
20. kinetic, thermodynamic, structural and ultrastructural data for characterization of mutant isomerase structures and for the TPI-related metabolic processes in normal and deficient cells PMID: 12023819
21. Minor structural changes in a mutated human melanoma antigen (TPI) correspond to dramatically enhanced stimulation of a CD4+ tumor-infiltrating lymphocyte line. PMID: 12051920
22. A patient with triosephosphate isomerase (TPI) deficiency exhibited worsening of abnormal involuntary movements of the dystonic type and developed psychiatric symptoms while on selegiline. PMID: 14743370
23. IgG-type anti-TPI autoantibodies were detected in 24.7% of the serum samples and 24.1% of the synovial fluid samples from the patients with osteoarthritis PMID: 15146421
24. anti-TPI antibodies are closely associated with neuropsychiatric lupus PMID: 15358119
25. We found that a low TPI activity in the mutant cells (lower than predicted from the protein level and specific activity of the purified recombinant enzyme) is coupled with an increase in the activities of glycolytic kinases PMID: 16086671
26. Mutations causing TPI deficiency in humans are characterized by progressive neurological dysfunction, neurodegeneration, and early death. PMID: 17008404
27. TPI and GAPDH may be candidate Ags for an autoimmune response to neurons and axons in multiple sclerosis. PMID: 17015754
28. anti-TPI form immune complexes in CSF and contribute to the pathogenesis of neuropsychiatric lupus by activating the complement system PMID: 17064784
29. Triosephosphate isomerase (TPI), a glycolytic pathway enzyme, was identified as a downregulated protein in SGC7901/VCR cells PMID: 18309519
30. TPI variants occur less frequent than expected and inactive alleles are not enriched in German centenarians PMID: 18510744
31. human triosephosphate isomerase mutation E104D is related to alterations of a conserved water network at the dimer interface PMID: 18562316
32. Population samples from Angola, Mozambique and S. Tome e Principe has 3 haplotypes of the TPI gene promoter variants -5A-8G-24T,-5G-8G-24T and -5G-8A-24T in malaria-infected individuals. PMID: 18792062
33. This protein has been found differentially expressed in the Wernicke's Area from patients with schizophrenia. PMID: 19405953
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相關疾病：

Triosephosphate isomerase deficiency (TPID)
亞細胞定位：

Cytoplasm.
蛋白家族：

Triosephosphate isomerase family
數據庫鏈接：

HGNC: 12009

OMIM: 190450

KEGG: hsa:7167

STRING: 9606.ENSP00000229270

UniGene: Hs.524219

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