TALDO1 Antibody
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货号:CSB-PA04275A0Rb
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规格:¥440
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促销:
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图片:
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Immunohistochemistry of paraffin-embedded human placenta tissue using CSB-PA04275A0Rb at dilution of 1:100
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Immunohistochemistry of paraffin-embedded human lung tissue using CSB-PA04275A0Rb at dilution of 1:100
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Western blot
All lanes: TALDO1 antibody at 0.1µg/ml
Lane 1: Human placenta tissue
Lane 2: Hela whole cell lysate
Lane 3: Jurkat whole cell lysate
Lane 4: A375 whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 38 kDa
Observed band size: 38 kDa
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) TALDO1 Polyclonal antibody
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Uniprot No.:P37837
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基因名:TALDO1
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别名:Dihydroxyacetone transferase antibody; EC 2.2.1.2 antibody; EPS8L2 antibody; Glycerone transferase antibody; TAL antibody; TAL H antibody; TALDO antibody; TALDO_HUMAN antibody; TALDO1 antibody; TALDOR antibody; TALH antibody; Transaldolase 1 antibody; Transaldolase antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Transaldolase protein (9-337AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,TALDO1 Antibody (CSB-PA04275A0Rb),的标记方式是Non-conjugated。对于TALDO1 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:2000 IHC 1:20-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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.
相关产品
靶点详情
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功能:Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway.
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基因功能参考文献:
- These results demonstrate that the nucleocytoplasmic distribution of TALDO1, modulated via alternative translational initiation and dimer formation, plays an important role in a wide range of metabolic networks PMID: 27703206
- The above findings support the premise that biallelic mutations in TALDO1 are responsible for transaldolase deficiency and confirm the broad phenotypic variability of this condition, even with the same genotype. PMID: 25388407
- This study expands the clinical definition of transaldolase deficiency, and adds to its allelic heterogeneity. PMID: 23315216
- Data suggest that exchange reactions during gluconeogenesis catalyzed by transaldolase and triose-phosphate isomerase do not differ between subjects with type 2 diabetes and control subjects under fasting or hyperglycemic conditions. PMID: 23736541
- renal phenotype of patients with transaldolase deficiency PMID: 22510381
- these data provide strong experimental evidence that transaldolase exchange occurs in humans, resulting in an overestimate of gluconeogenesis PMID: 21062960
- Data show that erythronic acid was identified as a major abnormal metabolite in all patients and in knock-out TALDO mice implicating an as yet unknown biochemical pathway in this disease. PMID: 20600873
- granzyme B-cleaved transaldolase-specific T cell-mediated cytotoxicity may contribute to the progressive destruction of oligodendrocytes in patients with multiple sclerosis PMID: 20194725
- transaldolase is regulated by ZNF143 in a tissue-specific manner PMID: 14702349
- TALase undergoes anterograde trafficking in neutrophils from nonpregnant individuals, whereas retrograde trafficking is found during pregnancy PMID: 16092052
- Mutation in the TALDO1 gene was found in patients with hydrops fetalis and neonatal multi-organ disease. PMID: 17095351
- A patch of functionally important amino acid residues extends from serine-171 toward the catalytic site and is proposed as a novel ligand shuttling path connecting these specific sites to the enzyme's active site. PMID: 17503352
- Transaldolase-deficient patients had significantly increased urinary heptoses, revealing novel urinary biomarkers for identification of the deficiency. PMID: 17603756
- A new case of TALDO deficiency resulted in cirrhosis, rickets and deafness. PMID: 18331807
- The present study identified the TAL deficiency as a modulator of mitochondrial homoeostasis, Ca(2+) fluxing and apoptosis. PMID: 18498245
- analysis of enzymes TalB and Taldo1 in human and E. coli PMID: 18687684
- genetic polymorphisms in Transaldolase 1 are associated with squamous cell carcinoma of the head and neck . PMID: 18805652
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收起更多
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相关疾病:Transaldolase deficiency (TALDOD)
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亚细胞定位:Cytoplasm.
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蛋白家族:Transaldolase family, Type 1 subfamily
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数据库链接:
HGNC: 11559
OMIM: 602063
KEGG: hsa:6888
STRING: 9606.ENSP00000321259
UniGene: Hs.438678
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