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抗坏血酸-6-棕榈酸酯号：137-66-6   
英文名称：Ascorbyl palmitate；L-Ascorbyl 6-palmitate；6-O-Palmitoyl-L-ascorbic acid；Ascorbic acid 6-palmitate   
其他名称：L-抗坏血酸棕榈酸酯；*棕榈酸酯   
号：137-66-6   
C22H38O7= 414.53   
级别：BR   
含量：≥95.0%    
比旋光度：+23±1°（c=1% in ethanol）   
熔点：113～117℃   
干燥失重：≤0.2%   
性状(以下信息仅供参考)：白色粉末，略有柑橘气味极易溶于水和植物油，易熔于乙醇   
用途：本品仅供科研，不得用于其它用途   
保存：RT 抗坏血酸-6-棕榈酸酯号：137-66-6储存条件：
避光、干燥阴凉处封闭贮存,严禁与有毒、有害物品混放、混运。本品为非危险 产品可按一般化学品运输,轻搬动轻放,防止日晒、雨淋！受热、受潮、受光后易丧失活力,保存期短,因此贮存和运输条件比较苛刻。
运输：汽车运输、EMS邮政快递，申通快递等， 款到上海3天内发货；
售后：如您对我们的产品服务及技术指标有特殊要求，请及时通知我方。
存储：应贮存在干燥清洁避光的环境中，严禁与有毒物质混放，以免污染（保质期为两年）。
抗坏血酸-6-棕榈酸酯号：137-66-6主要优级纯、分级纯和化学纯3种：
（1）优级纯（GR：Guaranteed reagent），又称一级品或保证试剂，99.8%，这种试剂纯度Z高，杂质含量Z低，适合于重要精密的分析工作和科学研究工作，使用绿色瓶签。
（2）分析纯（AR），又称二级试剂，纯度很高，99.7%，略次于优级纯，适合于重要分析及一般研究工作，使用红色瓶签。
（3）化学纯（CP），又称三级试剂，≥ 99.5%，纯度与分析纯相差较大，适用于工矿、学校一般分析工作。使用蓝色（深蓝色）标签。
（4）实验试剂（LR：Laboratory reagent），又称四级试剂。

抗体来源  Rabbit 
克隆类型  polyclonal
交叉反应  Human, Mouse, Rat, Cow, Rabbit, Sheep
产品类型  一抗   
研究领域 
性    状  Lyophilized or Liquid
免 疫 原  KLH conjugated synthetic peptide derived from human SP-C Propeptide
亚    型  IgG
纯化方法  affinity purified by Protein A
储 存 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
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  ICC=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 This gene encodes the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 2, also called pulmonary alveolar proteinosis due to surfactant protein C deficiency, and are associated with interstitial lung disease in older infants, children, and adults. Alternatively spliced transcript variants encoding different protein isoforms have been identified.
Function : Pulmonary surfactant associated proteins promote alveolar stability by lowering the surface tension at the air-liquid interface in the peripheral air spaces.
Subcellular Location : Secreted, extracellular space, surface film.
DISEASE : Defects in SFTPC are the cause of pulmonary surfactant metabolism dysfunction type 2 (SMDP2) [MIM:610913]; also called pulmonary alveolar proteinosis due to surfactant protein C deficiency. A rare disease associated with progressive respiratory insufficiency and lung disease with a variable clinical course, due to impaired surfactant homeostasis. It is characterized by alveolar filling with floccular material that stains positive using the periodic acid-Schiff method and is derived from surfactant phospholipids and protein components. Excessive lipoproteins accumulation in the alveoli results in severe respiratory distress.
Genetic variations in SFTPC are a cause of susceptibility to respiratory distress syndrome in premature infants (RDS) [MIM:267450]; also known as RDS in prematurity. RDS is a lung disease affecting usually premature newborn infants. It is characterized by deficient gas exchange, diffuse aectasis, high-permeability lung edema and fibrin-rich alveolar deposits called 'hyaline membranes'.
Similarity : Contains 1 BRICHOS domain.
抗坏血酸-6-棕榈酸酯号：137-66-6Database links : UniProtKB/Swiss-Prot: P11686.2
英文名称  Anti-Syndecan 3
中文名称  Syndecan 3蛋白抗体
别    名  N-syndecan; Sdc3; SDC3_HUMAN; SDCN; SYND3; syndecan proteoglycan 3; Syndecan-3. 
浓    度  1mg/1ml
规 格  0.1ml/100μg  0.2ml/200μg
抗体来源  Rabbit 
克隆类型  polyclonal
交叉反应  Human  
产品类型  一抗   
研究领域  细胞生物 免疫学 信号转导 
蛋白分子量  predicted molecular weight: 45kDa
性    状  Lyophilized or Liquid
免 疫 原  KLH conjugated synthetic peptide derived from human Syndecan 3
亚    型  IgG
纯化方法  affinity purified by Protein A
储 存 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
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  ICC=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 Syndecan 3 is a belongs to the syndecan proteoglycan family. It may play a role in the organization of cell shape by affecting the actin cytoskeleton, possibly by transferring signals from the cell surface in a sugar-dependent mechanism. Allelic variants of this gene have been associated with obesity.
Function : Cell surface proteoglycan that may bear heparan sulfate (By similarity). May have a role in the organization o