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AP192SA6

驴抗小鼠IgG,Alexa Fluor 647结合物,吸附物:H,R,B,Eq,Gt,Sh,Rb,Ch,Gp抗体

Chemicon®

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
ALEXA FLUOR 647
Clone:
polyclonal
Application:
immunofluorescence
Species reactivity:
mouse
Citations:
7
Technique(s):
immunofluorescence: suitable
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产品名称

驴抗小鼠IgG,Alexa Fluor 647结合物,吸附物:H,R,B,Eq,Gt,Sh,Rb,Ch,Gp抗体, Chemicon®

biological source

donkey

conjugate

ALEXA FLUOR 647

antibody product type

secondary antibodies

clone

polyclonal

species reactivity

mouse

packaging

pkg of 0.5 mg

manufacturer/tradename

Chemicon®

technique(s)

immunofluorescence: suitable

shipped in

wet ice

Quality Level

Application

用 dH2O 将产品重悬至 1.4 mg/mL。
对于大多数应用,建议的稀释范围:1:100 – 1:800.
最佳工作稀释度必须由最终用户确定。
研究子类别
用于双重标记的吸附的二抗
研究类别
神经科学
驴抗小鼠 IgG,Alexa Fluor 647 结合物,吸附的物种:H、R、B、Eq、Gt、Sh、Rb、Ch、Gp 抗体是抗小鼠 IgG 的抗体,用于免疫荧光。

Biochem/physiol Actions

基于免疫电泳和/或 ELISA,该抗体与全分子小鼠 IgG 反应。 它还与其他小鼠免疫球蛋白的轻链反应。 未检测到抗非免疫球蛋白血清蛋白的抗体。
该抗体已通过 ELISA 测试和/或固相吸收,以确保与牛、鸡、山羊、豚鼠、叙利亚仓鼠、马、人、兔、大鼠和绵羊的血清蛋白交叉反应最小,但可能会与其他物种的免疫球蛋白发生交叉反应。

Disclaimer

除非我们的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于人类或动物。

General description

Alexa Fluor 647 偶联的 AffiniPure 驴抗小鼠 IgG(H + L)(与牛、鸡、山羊、豚鼠、叙利亚仓鼠、马、人、兔、大鼠和绵羊血清蛋白具有最小的交叉反应)。

Immunogen

荧光团信息
Alexa Fluor 647 羧酸
Amax = 651;Emax = 667
荧光团/蛋白质吸收率:A651/A280=4.5

Physical form

在含有 0.01M 磷酸钠,0.25M NaCl,pH 7.6 和 15 mg/mL BSA 和 0.05% 叠氮化钠的缓冲液中冻干。
该抗体是使用与琼脂糖珠偶联的抗原,通过免疫亲和色谱法从抗血清中的纯化的。

Preparation Note

自收到之日起,在冻干后在 2-8ºC 可稳定保存 1 年。
重悬后,该产品作为稀释液在 2-8°C 可稳定保存数周。要延长重悬后溶液的保存时间,请添加等体积的甘油,使甘油的终浓度达到 50%,然后以未稀释的等分试样置于 -20°C 下可保存长达 12 个月。请注意,添加甘油后,蛋白质(和缓冲盐)的浓度将降至原浓度的一半。应避免反复冻/融循环。

Legal Information

ALEXA FLUOR is a trademark of Life Technologies
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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hcodes

Hazard Classifications

Aquatic Chronic 3

存储类别

11 - Combustible Solids

wgk

WGK 3


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Chencheng Feng et al.
International journal of molecular medicine, 41(6), 3316-3326 (2018-03-08)
Intervertebral disc (IVD) degeneration (IDD) is a widely recognized contributor to low back pain. Mechanical stress is a crucial etiological factor of IDD. During the process of IDD, a vicious circle is formed between abnormal mechanical stress and the damage
Yongliang Wang et al.
Journal of biophotonics, 12(5), e201800351-e201800351 (2018-11-30)
Nucleases are important enzymes that cleave nucleic acids and play critical roles in DNA repair, immune defense and potentially in cancer invasion. However, their spatial dynamics at subcellular level is much less studied. Here, we developed a surface-tethered nuclease sensor
Chencheng Feng et al.
Oxidative medicine and cellular longevity, 2017, 7426458-7426458 (2017-11-18)
Senescence is a crucial driver of intervertebral disc degeneration (IDD). Disc cells are exposed to high oxygen tension due to neovascularization in degenerative discs. However, the effect of oxygen tension on disc cell senescence was unknown. Herein, rat nucleus pulposus
Tianlong Zhang et al.
Nature communications, 8(1), 1394-1394 (2017-11-11)
Amino acid-dependent activation of the mechanistic target of rapamycin complex 1 (mTORC1) is mediated by Rag GTPases, which are recruited to the lysosome by the Ragulator complex consisting of p18, MP1, p14, HBXIP and C7orf59; however, the molecular mechanism is
Anwesha Sarkar et al.
Physical biology, 15(6), 065002-065002 (2018-05-23)
Integrin-transmitted cellular forces are crucial mechanical signals regulating a vast range of cell functions. Although various methods have been developed to visualize and quantify cellular forces at the cell-matrix interface, a method with high performance and low technical barrier is

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