SAB4200119
单克隆抗 FLAG过氧化物酶 大鼠抗
2-4 mg/mL, clone 6F7, purified immunoglobulin
别名:
抗 ddddk, 抗 dykddddk
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关于此项目
NACRES:
NA.32
UNSPSC Code:
12352203
Conjugate:
peroxidase conjugate
Clone:
6F7, monoclonal
Application:
western blot
Species reactivity:
all
Citations:
9
Technique(s):
western blot: 1:1,000-1:2,000 using extracts of transfected cells expressing C-terminal FLAG-tagged fusion protein
产品名称
单克隆抗 FLAG过氧化物酶 大鼠抗, 2-4 mg/mL, clone 6F7, purified immunoglobulin
biological source
rat
conjugate
peroxidase conjugate
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
6F7, monoclonal
form
buffered aqueous solution
species reactivity
all
concentration
2-4 mg/mL
technique(s)
western blot: 1:1,000-1:2,000 using extracts of transfected cells expressing C-terminal FLAG-tagged fusion protein
isotype
IgG1
immunogen sequence
DYKDDDDK
shipped in
dry ice
storage temp.
−20°C
Quality Level
Application
单克隆抗FLAG过氧化物酶可识别N端、C端和内部FLAG标签融合蛋白。特别推荐该产品用于识别C-端FLAG标签融合蛋白。该产品可用于免疫印迹。
更多产品信息，请访问我们的FLAG®应用页面。
General description
单克隆抗FLAG过氧化物酶是从生长于生物反应器中的6F7杂交瘤细胞培养上清中分离出来、与辣根过氧化物酶（HRP）偶联的单克隆抗FLAG（大鼠IgG1同种型）的免疫球蛋白纯化级分。杂交瘤6F7是FLAG肽免疫大鼠的骨髓瘤细胞和脾细胞融合产生的。
该产品可识别N端、C端和内部FLAG标签融合蛋白。特别推荐用于识别C端FLAG标签融合蛋白。
Immunogen
从生长于生物反应器中的6F7杂交瘤细胞培养上清中分离出来、与辣根过氧化物酶（HRP）偶联的单克隆抗FLAG（大鼠IgG1同种型）的免疫球蛋白纯化级分。
Physical form
溶解在0.01M磷酸缓冲盐,pH7.4, 含有0.01%硫柳汞。
Legal Information
FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
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存储类别
10 - Combustible liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
常规特殊物品
此项目有
Claudia Isabelle Keller Valsecchi et al.
Nature, 589(7840), 137-142 (2020-11-20)
Confinement of the X chromosome to a territory for dosage compensation is a prime example of how subnuclear compartmentalization is used to regulate transcription at the megabase scale. In Drosophila melanogaster, two sex-specific non-coding RNAs (roX1 and roX2) are transcribed
Jasjot Singh et al.
Nature communications, 13(1), 6212-6212 (2022-10-21)
Lysosomes are well-established as the main cellular organelles for the degradation of macromolecules and emerging as regulatory centers of metabolism. They are of crucial importance for cellular homeostasis, which is exemplified by a plethora of disorders related to alterations in
Meidi Gu et al.
Nature immunology, 22(2), 193-204 (2021-01-06)
Metabolic reprograming toward aerobic glycolysis is a pivotal mechanism shaping immune responses. Here we show that deficiency in NF-κB-inducing kinase (NIK) impairs glycolysis induction, rendering CD8+ effector T cells hypofunctional in the tumor microenvironment. Conversely, ectopic expression of NIK promotes
Jente Stouthamer et al.
Methods in molecular biology (Clifton, N.J.), 2690, 193-204 (2023-07-14)
Interactions between extracellular domains (ECDs) are crucial for many physiological processes in the cell, most importantly perception of its environment. However, studying these often-transient interactions can be challenging. Here we describe a method that allows for in vitro detection of
W R Force et al.
The Journal of biological chemistry, 275(15), 11121-11129 (2001-02-07)
Lymphotoxin-beta receptor (LTbetaR), a member of the tumor necrosis factor receptor superfamily, is essential for the development and organization of secondary lymphoid tissue. Wild type and mutant LTbetaR containing successive truncations of the cytoplasmic domain were investigated by retrovirus-mediated gene
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