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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
- Neuron-Specific Enolase (NSE-P1)保存于运输说明:
- Store at -20°C
- 详细信息:
-
Description 
Monoclonal Antibody against Neuron-Specifc Enolase, clone NSE-P1 Intended Use 
**Research Use Only (RUO)**
This product is sold for laboratory research use only, not for human or in-vivo use.Clone 
NSE-P1 Form 
Neuron-Specific Enolase (NSE-P1)Purified Antibody (in PBS + 0.03% thimerosal) Host 
Mouse IsoType 
IgG1 [Ab] 
1 mg/mL Specificity 
Neuron specific enolase is found in elevated concentrations in plasma and certain neoplasias. These include pediatric neuroblastoma and small cell lung cancer. This antibody was raised against a synthetic peptide corresponding to amino acids 416-433. It recognizes the sequence LGDEARFAGHNFRNPSVL. The antiserum was purified against a protein G column. Uses 
Neuron-Specific Enolase (NSE-P1)This antibody is effective in ELISA, immunoblotting and immunohistochemistry. Suggested Working Dilution 
The optimal working dilution should be determined for each specific assay condition. - Western blot: 1:1,000*
- ELISA: 1:500
Notes 
* Predicted MW = 47kDa Storage 
Store at -20°C. Upon initial thawing, apportion into working aliquots and store at -20°C. Avoid repeated freeze-thaw cycles to prevent denaturing the antibody. For long-term storage, keep the antibody at -80°C. References 
Murray GI, Duncan ME, Melvin WT, Fothergill JE. Immunohistochemistry of neurone specific enolase with gamma subunit specific anti-peptide monoclonal antibodies. J Clin Pathol 46:993-996, 1993.
Duncan ME, McAleese SM, Booth NA, Melvin WT, Fothergill JE. A simple enzyme-linked immunosorbent assay (ELISA) for the neuron-specific gamma isozyme of human enolase (NSE) using monoclonal antibodies raised against synthetic peptides corresponding to isozyme sequence differences. J Immuno Methods 151:227-236, 1992.Warranty/Conditions 
Covance products may not be resold or modified for resale without prior written approval. - Neuron-Specific Enolase (NSE-P1)
- xy-0065xy SP (Substance P)P物质(抗原)
xy-3970xy SDHA琥珀酸脱氢酶复合体亚基A
xy-1175xy SHBG性激素结合球蛋白多肽
xy-0437xy-xyy5 Streptavidin/Cy5荧光素Cy5标记链霉亲和素
xy-0437xy Streptavidin, SA链霉亲和素
xy-2410xy SHBG性激素结合球蛋白多肽
xy-0726xy Survivin细胞凋亡抑制因子4(抗原)
xy-2037xyA streptomycin/OVA链霉素偶联鸡卵白蛋白
xy-0291xy THY (thyroglobulin,TG)甲状腺球蛋白
xy-0973xyB Tetracycline/BSA四环素偶联牛血清白蛋白
xy-6190xy Thyroxine Binding Globulin甲状腺素结合球蛋白抗原
xy-0973xyA Tetracycline/OVA四环素偶联鸡卵白蛋白
xy-0357xy TRH (Thyrotropin releasing hormone )促甲状腺素释放激素
xy-0392xy Thymopentin胸腺五肽
xy-0706xyB T4-BSA甲状腺素T4偶联牛血清白蛋白
xy-0387xy rh-TNF-Alpha(rh-Tumor Necrosis Factor alpha)重组人肿瘤坏死因子
xy-1411xy TERT端粒酶逆转录酶
xy-0865xy Tachyplesin I(Tachyplesin-1 precursor )抗菌肽
xy-1211xy TOP1MT拓普西异构酶Ⅰ抗原
xy-2052xy Transferrin转铁蛋白
xy-1215xy TPH色氨酸羟化酶(多肽)
xy-6308xy UACA葡萄膜自身抗原Uaca
xy-2041xy YFV Envelope glycoprotein黄热病毒包膜糖蛋白
xy-0861xyB 2,4-D/BSA2,4-二氯苯氧乙酸偶联牛血清白蛋白
xy-1930xy ADH/AVP peptide抗利尿激素/血管升压素抗原(和肽素)
xy-4507xy PRRSV M protein猪蓝耳病病毒M蛋白
xy-4814xy-HRxy Newcastle disease virus/HRP鸡新城疫疫苗(鸡瘟4型混合病毒)偶联辣根过氧化物酶
xy-0645xy sIgA大鼠分泌型IgA(抗原)
xy-2036xyB Penicillin G/BSA青霉素G偶联牛血清白蛋白
xy-2036xyA Penicillin G/OVA青霉素G偶联鸡卵白蛋白
xy-1077xy OCT2 (Octamer-binding transcription factor 2)阳离子转运蛋白2抗原
六、标记蛋白质与多肽
编号 名 称
xy-4560xyB Taurine/BSA牛磺酸偶联牛血清白蛋白(β-氨基乙磺酸)
xy-0292xy-xyy5 BSA/Cy5荧光素Cy5标记牛血清白蛋白
xy-0292xy-xyy5.5 BSA/Cy5.5荧光素Cy5.5标记牛血清白蛋白
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文献和实验Characterization of P1 (Adenosine) Purinoceptors
Figure 1.9.1 (A ) Representative autoradiographic image of specific [3 H]CHA (1 nM) binding to rat brain sagittal sections (Jarvis, ). (B ) Representative autoradiographic image of specific [3 H]CGS 21680 (5 nM) binding to ADO A2A receptors
Assembling New Escherichia coli Strains by Transduction Using Phage P1
a locus to wild type, to move specific genetic markers from one strain to another, to relocate different mutant genes to a common genetic background, and to evaluate second-site suppression of a mutant allele. Because of these abilities, P1 transduction
Site-Specific Gene Integration in Rice
genomic position can be obtained by employing site-specific recombination systems derived from bacteria or yeast. P1 bacteriophage Cre-lox system has been particularly successful in directing precise integration of foreign genes into “previously engineered
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