D-果糖-1，6-二磷酸三钠号：38099-82-0

公司提供的D-果糖-1，6-二磷酸三钠号：38099-82-0*，货源充足。严格的生产质量控制体系，包括：优级纯，分析纯，化学纯，试剂级，基准试剂，实验纯，教学试剂，高纯试剂，色谱纯，光谱纯，电子纯。各种包装规格，并可提供包装定制，咨询订购。
D-果糖-1，6-二磷酸三钠号：38099-82-0   
英文名称：FDP ；D-Fructose-1，6-Phosphate trisodium salt；Harden-Young ester；Hexose diphosphate trisodium salt；D(+)Fructofuranose 1,6-diphosphate trisodium salt    
其他名称：1，6-二磷酸果糖三钠盐   
号：38099-82-0   
C6H11Na3O12P2=406.06   
级别：试剂级   
含量：≥98.0%   
干燥失重：25～28%   
性状(以下信息仅供参考)：白色或类白色粉末   
用途：本品仅供科研，不得用于其它用途   
保存：-20℃客户根据D-果糖-1，6-二磷酸三钠号：38099-82-0性质、化学式、分子式、结构式、比重、密度、号、沸点、熔点、水溶性、MSDS、用途、作用、规格包装、性状、注意事项、英文名、别称、纯度、级别等情况，本产品化学性质稳定，运输条件不苛刻，一般储存在阴凉，干燥，通风良好的地方，远离不相容的物质。保持容器密闭。
试剂品牌：TCI、sigma、Alfa、Avocado、Aldrich、ACROS、Fluka、ICN（MP）等
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抗体来源  Rabbit 
克隆类型  polyclonal
交叉反应  Human, Mouse, Rat, Dog, Pig, Cow, Guinea Pig, G 
产品类型  一抗  磷酸化抗体  
研究领域  肿瘤 免疫学 神经生物学 细胞膜受体 新陈代谢 
蛋白分子量  predicted molecular weight: 73kDa
性    状  Lyophilized or Liquid
免 疫 原  KLH conjugated Synthesised phosphopeptide derived from human SCNN1B around the phosphorylation site of Ser633
亚    型  IgG
纯化方法  affinity purified by Protein A
储 存 液  0.01M PBS, pH 7.4 with 10 mg/ml BSA and 0.1% Sodium azide
产品应用   WB=1:100-500  ELISA=1:500-1000  IP=1:20-100  IHC-P=1:100-500  IHC-F=1:100-500  Flow-Cyt=1:100-500  IF=1:100-500
（石蜡切片需做抗原修复）
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user. 
保存条件  Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍 SCNN1B is a subunit of the epithelial sodium channel, ENaC. ENac has high sodium selectivity, low conductance, and amiloride sensitivity. The functional channel of ENaC is composed of at least 3 subunits, alpha (SCNN1A), beta (SCNN1B), and gamma (SCNN1G). The 3 subunits show sequence similarities to one another, indicating descent from a common ancestral gene. Each encodes a protein containing 2 transmembrane domains, with intracellular amino and carboxyl termini.
Function : Sodium permeable non-voltage-sensitive ion channel inhibited by the diuretic amiloride. Mediates the electrodiffusion of the luminal sodium (and water, which follows osmotically) through the apical membrane of epithelial cells. Controls the reabsorption of sodium in kidney, colon, lung and sweat glands. Also plays a role in taste perception.
Subunit : Probable heterotrimer containing one alpha, one beta and one gamma subunit. A delta subunit D-果糖-1，6-二磷酸三钠号：38099-82-0can replace the alpha subunit. Interacts with the WW domains of NEDD4, NEDD4L, WWP1 and WWP2. Interacts with the full length immature form of PCSK9 (pro-PCSK9).
Subcellular Location : Apical cell membrane; Multi-pass membrane protein. Note=Apical membrane of epithelial cells.
Post-translational modifications : Phosphorylated on serine and threonine residues (By similarity).
DISEASE : Pseudohypoaldosteronism 1, autosomal recessive (PHA1B) [MIM:264350]: A rare salt wasting disease resulting from target organ unresponsiveness to mineralocorticoids. PHA1B is a severe form involving multiple organ systems, and characterized by an often fulminant presentation in the neonatal period with dehydration, hyponatremia, hyperkalemia, metabolic acidosis, failure to thrive and weight loss. Note=The disease is caused by mutations affecting the gene represented in this entry. The degree of channel function impairment differentially affects the renin-aldosterone system and urinary Na/K ratios, resulting in distinct genotype-phenotype relationships in PHA1 patients. Loss-of-function mutations are associated with a severe clinical course and age-dependent hyperactivation of the renin-aldosterone system. This feature is not observed in patients with missense mutations that reduce but do not eliminate channel function. Markedly reduced channel activity results in impaired linear growth and delayed puberty (PubMed:18634878).
Liddle syndrome (LIDDS) [MIM:177200]: Autosomal dominant disorder characterized by pseudoaldosteronism and hypertension associated with hypokalemic alkalosis. The disease is caused by constitutive activation of the renal epithelial sodium channel. Note=The disease is caused by mutations affecting the gene represented in this entry.
Bronchiectasis with or without elevated sweat chloride 1 (BESC1) [MIM:211400]: A debilitating respiratory disease characterized by chronic, abnormal dilatation of the bronchi and other cystic fibrosis-like symptoms in the absence of known causes of bronchiectasis (cystic fibrosis, autoimmune diseases, ciliary dyskinesia, common variable immunodeficiency, foreign body obstruction). Clinical features include sub-normal lung function, sinopulmonary infections, chronic productive cough, excessive sputum production, and elevated sweat chloride in some cases. Note=The disease is caused by mutations affecting the gene represented in this entry.
Similarity : Belongs to the amiloride-sensitive sodium channel (TC 1.A.6) family. SCNN1B subfamily.
Database links :
UniProtKB/Swiss-Prot: P51168.2
Entrez Gene: 6338 Human
Omim: 600760 Human
SwissProt: P51168 Human
Unigene: 414614 Human
英文名称  Anti-SPRN
中文名称  新朊蛋白抗体（C端）
别    名  rCG47959; shadow of prion protein; SHO; Protein shadoo; bA108K14.1; C630041J07; FLJ41197; SPRN; Shadow of prion protein precursor; SPRN_MOUSE.
浓    度  1mg/1ml
规 格  0.2ml/200μg
抗体来源  Rabbit 
克隆类型  polyclonal
交叉反应  Mouse, Rat
产品类型  一抗   
研究领域  免疫学 神经生物学 细胞凋亡 
蛋白分子量  predicted molecular weight: 12kDa
性    状  Lyophilized or Liquid
免 疫 原  KLH conjugated synthetic peptide derived from mouse Shadow(CT)
亚    型  IgG
纯化方法  affinity purified by Protein A
储 存 液  0.01M PBS, pH 7.4 with 10 mg/ml BSA and 0.1% Sodium azide
产品应用   WB=1:100-500  ELISA=1:500-1000  IP=1:20-100  IHC-P=1:100-500  IHC-F=1:100-500  IF=1:100-500
（石蜡切片需做抗原修复）
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user. 
保存条件  Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.