biological source
mouse
Quality Level
conjugate
ALEXA FLUOR™ 488
antibody form
purified antibody
antibody product type
primary antibodies
clone
9E10, monoclonal
species reactivity (predicted by homology)
all
manufacturer/tradename
Upstate®
technique(s)
immunocytochemistry: suitable, western blot: suitable
isotype
IgG1
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Gene Information
human ... MYC(4609)
General description
变化
Immunogen
对应于人Myc（AEEQKLISEEDLLRKRREQLKHKLEQ-LRNS）亮氨酸拉链区氨基酸408-437的合成肽。
Application
研究子类别
表位标签
表位标签
研究类别
表位标签 & 一般用途
表位标签 & 一般用途
该抗-Myc标签抗体（克隆9E10），Alexa Fluor 488 偶联物经验证可用于WB、 IC检测Myc 标签。
Biochem/physiol Actions
Myc和含有Myc表位标签的重组蛋白。
Physical form
蛋白G纯化
Preparation Note
自发货之日起在4°C下可保存1年
Analysis Note
通过免疫细胞化学法对Myc标记重组蛋白进行了常规评估
Legal Information
ALEXA FLUOR is a trademark of Life Technologies
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Alexa Fluor™是Molecular Probes, Inc.的注册商标。
除非在产品目录或产品附带的其他公司文档另有说明，否则我们的产品仅供研究使用，不得对人或动物用于任何其他目的，包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用。
除非在产品目录或产品附带的其他公司文档另有说明，否则我们的产品仅供研究使用，不得对人或动物用于任何其他目的，包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用。
Still not finding the right product?
试用我们的 产品选型工具 工具缩小选择范围
存储类别
12 - Non Combustible Liquids
wgk
WGK 2
Xavier Charest-Morin et al.
Peptides, 60, 71-79 (2014-08-17)
Based on the known fact that the parathyroid hormone (PTH) might be extended at its C-terminus with biotechnological protein cargoes, a vector directing the secretion of PTH1-84 C-terminally fused with the antigenic epitope myc (PTH-myc) was exploited. The functional properties
Ashwani Sharma et al.
Traffic (Copenhagen, Denmark), 22(10), 332-344 (2021-08-22)
Smith-Lemli-Opitz syndrome (SLOS) is a congenital and developmental malformation syndrome associated with defective cholesterol biosynthesis. It is characterized by accumulation of 7-dehydrocholesterol (the immediate biosynthetic precursor of cholesterol in the Kandutsch-Russell pathway) and an altered cholesterol to total sterol ratio.
Arsen S Hunanyan et al.
Human gene therapy, 32(7-8), 405-419 (2021-02-13)
Alternating Hemiplegia of Childhood (AHC) is a devastating autosomal dominant disorder caused by ATP1A3 mutations, resulting in severe hemiplegia and dystonia spells, ataxia, debilitating disabilities, and premature death. Here, we determine the effects of delivering an extra copy of the
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 16-308 | 04053252627200 |