- ￥4700
- GeneTex
- 美国
- GTX13824
- 2025年07月11日
- WB, ICC/IF, IHC-P, IP, IHC, PLA
- Mouse
- Human, Mouse
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant Aurora-A
- 亚型：
IgG2b
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性：
Monoclonal
- 标记物：
Unconjugated
- 适应物种：
Human, Mouse
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX13824
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Mouse
- 应用范围：
WB, ICC/IF, IHC-P, IP, IHC, PLA
- 浓度：
1.0 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
This antibody recognizes an epitope within the non-catalytic N-terminal domain of Aurora A. Clone 35C1 does not inhibit Aurora A kinase activity (Cremet et al. 2003).
- 抗体英文名：
Aurora A antibody [35C1]
- 抗体名：
Aurora A 抗体 [35C1]
- 规格：
50 μg
WB analysis of Aurora A kinase recombinant protein using GTX13824 Aurora A antibody
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文献和实验Pakala SB et al., J Biol Chem 2012 (PMID:23055517)
Wuputra K et al., Int J Mol Sci 2022 (PMID:35887129)
P?rez-Fidalgo JA et al., ESMO Open 2020 (PMID:33087400)
Lai CH et al., Cancer Lett 2020 (PMID:31875524)
Aradottir M et al., J Pathol Clin Res 2015 (PMID:27499891)
Wang YC et al., Exp Mol Med 2018 (PMID:29884818)
Wen QJ et al., Nat Med 2015 (PMID:26569382)
Richards MW et al., Proc Natl Acad Sci U S A 2016 (PMID:27837025)
Chang KC et al., PLoS One 2013 (PMID:24223200)
Yang F et al., Mod Pathol 2011 (PMID:21441901)
Goldenson B et al., Blood 2015 (PMID:25670627)
Margret Aradottir et al., The Journal of Pathology: Clinical Research 2014
Chen YP et al., Int J Cancer 2013 (PMID:24382688)
Yang G et al., Clin Cancer Res 2010 (PMID:20423983)
Yang G et al., Int J Cancer 2013 (PMID:23319376)
补体成分 C1(C1q/C1r/C1s) 补体成分：C1q 血清浓度(μg/ml)：75 分子量(kDa)：410 亚单位(链)及分子量(kDa)：A：24各6条B：23各6条C：22各6条 生物学活性：识别IgG、IgMFc的补体结合点 补体成分：C1r 血清浓度(μg/ml)：50 分子量(kDa)：85
35 Expression of Antibody Fab Fragments and Whole Immunoglobulin in Mammalian Cells
The technologies described in this volume enable the isolation of recombi- nant antibodies (Abs) from libraries of variable regions (Fvs) or Fabs displayed on the surface of filamentous phage by fusion to a structural protein
C1q Assay for the Detection of Complement Fixing Antibody to HLA Antigens
complement fixing from non-complement fixing antibody, the former of which are considered the most clinically relevant in the peri-transplant period. This chapter describes a novel solid phase C1q binding assay to distinguish HLA antibodies that can bind
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