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- 详细信息
- 文献和实验
- 技术资料
- 形态:
液态/粉状
- 保存条件:
-20℃保存
- 克隆性:
多克隆
- 标记物:
见说明书
- 适应物种:
人,大鼠,小鼠,兔
- 宿主:
Goat,Rabbit,Mouse
- 应用范围:
科研使用
- 浓度:
1mg/1ml
- 靶点:
来电咨询
1、制备抗原。
2、选择实验动物。
3、动物免疫。
4、试取血进行测试,看看是否成功免疫。
5、如果成功免疫,杀死实验动物,采集全部血清。
6、纯化出抗体。
7、鉴定抗体。包括纯度以及特异性。
ELISA夹心法测定中,HA与试剂抗体(捕获抗体和标记抗体)的结合,可通过Fc-Fc 和Fab-Fab两种结合方式干扰测定。正常情况下,在ELISA 夹心法中,待测抗原同时与捕获抗体和标记抗体结合,Phospho-eNOS (Ser1177) Antibody形成了固相捕获抗体-待测抗原-标记抗体的复合物(如图1A所示)。在以Fc-Fc 的方式结合的机制中,HA的Fc 端结合到捕获抗体的Fc 段上,而HA的Fab 区域则结合到标记抗体的Fab 区域上,导致假阳性结果(如图1B所示)。在以Fab-Fab 结合方式的机制可引起假阳性或假阴性的结果,如HA的Fab区域通过分别结合捕获抗体的Fab区域和标记抗体的Fab 区域,Phospho-eNOS (Ser1177) Antibody阻挡捕获抗体和标记抗体与待测抗原的结合,从而导致假阴性(如图1C所示);HA的F(ab’)2 通过同时结合捕获抗体的Fab区域和标记抗体的Fab区域,形成固相捕获抗体-HA-标记抗体复合物,如果标本中无待测抗原,HA就引起假阳性的结果。
Phospho-eNOS (Ser1177) Antibody:xy-0297G-xyy5.5 Goat Anti-human IgG/Cy5.5Cy5.5标记的羊抗人IgG
xy-0297G-xyE-xyy3 Goat Anti-human IgG/PE-Cy3PE-Cy3标记的羊抗人IgG
xy-0297G-xyE-xyY5 Goat Anti-human IgG/PE-CY5PE-CY5标记的羊抗人IgG
xy-0297G-Axyxy Goat Anti-human IgG/APCAPC标记的羊抗人IgG
xy-0297G-AF350 Goat Anti-human IgG/Alexa Fluor 350Alexa Fluor 350标记的羊抗人IgG
xy-0345G-RBITxy Goat Anti-human IgM/RBITC罗丹明标记的羊抗人IgM
xy-0345G-xyy5.5 Goat Anti-human IgM/Cy5.5Cy5.5标记的羊抗人IgM
xy-0345G-xyy7 Goat Anti-human IgM/Cy7Cy7标记的羊抗人IgM
xy-0345G-xyE Goat Anti-human IgM/PEPE标记的羊抗人IgM
xy-0345G-xyE-xyy3 Goat Anti-human IgM/PE-Cy3PE-Cy3标记的羊抗人IgM
xy-0345G-xyE-xyY5 Goat Anti-human IgM/PE-CY5PE-CY5标记的羊抗人IgM
xy-0345G-Axyxy Goat Anti-human IgM/APCAPC标记的羊抗人IgM
xy-0345G-AF350 Goat Anti-human IgM/Alexa Fluor 350Alexa Fluor 350标记的羊抗人IgM
xy-0345G-AF488 Goat Anti-human IgM/Alexa Fluor 488Alexa Fluor 488标记的羊抗人IgM
xy-0345G-AF555 Goat Anti-human IgM/Alexa Fluor 555Alexa Fluor 555标记的羊抗人IgM
xy-0345G-AF647 Goat Anti-human IgM/Alexa Fluor 647Alexa Fluor 647标记的羊抗人IgM
xy-0345G-xyE-xyy5.5 Goat Anti-human IgM/PE-Cy5.5PE-Cy5.5标记的羊抗人IgM
xy-0345G-xyE-xyy7 Goat Anti-human IgM/PE-Cy7PE-Cy7标记的羊抗人IgM
xy-0345G-xyy3 Goat Anti-human IgM/Cy3Cy3标记的羊抗人IgM
xy-0345G-Axy Goat Anti-human IgM/AP碱性磷酸酶(AP)标记的羊抗人IgM
xy-0345G-HRxy Goat Anti-human IgM/HRP辣根过氧化物酶标记的羊抗人IgM
xy-0297M-HRxy Mouse Anti-human IgG/HRP辣根过氧化物酶标记的小鼠抗人IgG
xy-0297M-Axy Mouse Anti-human IgG/AP碱性磷酸酶(AP)标记的小鼠抗人IgG
xy-0297M-RBITxy Mouse Anti-human IgG/RBITC罗丹明标记的小鼠抗人IgG
xy-0297M-FITxy Mouse Anti-human IgG/FITCFITC标记的小鼠抗人IgG
xy-0297M-Golxy Mouse Anti-human IgG/Gold胶体金标记的小鼠抗人IgG
xy-0297M-xyE-xyy5.5 Mouse Anti-human IgG/PE-Cy5.5PE-Cy5.5标记的小鼠抗人IgG
xy-0297M-xyE-xyy7 Mouse Anti-human IgG/PE-Cy7PE-Cy7标记的小鼠抗人IgG
xy-0297M-AF350 Mouse Anti-human IgG/Alexa Fluor 350Alexa Fluor 350标记的小鼠抗人IgG
xy-0297M-AF488 Mouse Anti-human IgG/Alexa Fluor 488Alexa Fluor 488标记的小鼠抗人IgG
xy-0297M-AF555 Mouse Anti-human IgG/Alexa Fluor 555Alexa Fluor 555标记的小鼠抗人IgG
xy-0297M-xyE-xyy3 Mouse Anti-human IgG/PE-Cy3PE-Cy3标记的小鼠抗人IgG
xy-0297M-xyE-xyY5 Mouse Anti-human IgG/PE-CY5PE-CY5标记的小鼠抗人IgG
xy-0297M-Axyxy Mouse Anti-human IgG/APCAPC标记的小鼠抗人IgG
xy-0297M-xyy3 Mouse Anti-human IgG/Cy3Cy3标记的小鼠抗人IgG
xy-0297M-xyy5 Mouse Anti-human IgG/Cy5Cy5标记的小鼠抗人IgG
xy-0297M-xyy5.5 Mouse Anti-human IgG/Cy5.5Cy5.5标记的小鼠抗人IgG
xy-0297M-xyy7 Mouse Anti-human IgG/Cy7Cy7标记的小鼠抗人IgG
Phospho-eNOS (Ser1177) Antibody单抗的最大优势是它的特异性、均一性、高效性和无限供应性。在免疫学、医学、生物学等领域的基础研究和临床医学上,包括对疾病(包括癌症)的诊断、预防和治疗等方面,均显示出巨大的生命力。
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文献和实验Using Phospho‐Motif Antibodies to Determine Kinase Substrates
comprising both the phosphorylated residue and the surrounding residues that determine kinase specificity, with degenerate residues taking up the remaining positions. Currently, several categories of phospho?motif antibody are commercially available
Optimized Protocol to Make Phospho-Specific Antibodies that Work
, not simply its level of expression. In this review, we will discuss both the design of the phosphopeptide immunogen and immunization. The affinity purification of the phospho-specific antibody as well as the methods most suitable for characterizing
Absorption Control in Immunohistochemistry Using Phospho-Peptides Immobilized on Magnetic Beads
neutralization of phospho-specific antibodies with phospho-peptides immobilized on magnetic beads. This technique allows for sequestration of antibody–peptide complex from the incubation solution, minimizing the risk of formation of unblocked antibodies capable
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