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Merck
CN

CBL162

抗-CD9抗体，克隆MM2/57

clone MM2/57, Chemicon®, from mouse

别名:

MRP-1, DRAP-27

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
MM2/57, monoclonal
Application:
flow cytometry
immunohistochemistry
immunoprecipitation (IP)
western blot
Species reactivity:
human, rabbit, mouse
Citations:
41
Technique(s):
flow cytometry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
Uniprot accession no.:
P21926

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产品名称

抗-CD9抗体，克隆MM2/57, clone MM2/57, Chemicon®, from mouse

biological source

mouse

conjugate

unconjugated

antibody form

purified antibody

antibody product type

primary antibodies

clone

MM2/57, monoclonal

species reactivity

human, rabbit, mouse

manufacturer/tradename

Chemicon®

technique(s)

flow cytometry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG2bκ

NCBI accession no.

NM_001769.2

UniProt accession no.

P21926

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

100

Gene Information

human ... CD9(928)

相关类别

Application

免疫组化： 血小板、单核细胞和前B细胞的冷冻切片，淋巴和上皮组织上有不同的染色
血小板抑制和聚集研究
必须由最终用户确定最佳工作稀释度。 最终用户。
抗CD9抗体，克隆MM2/57检测CD9的水平&，经发布 & 验证可用于FC、IP、WB、IH。
研究子类别
免疫球蛋白 & 免疫学
研究类别
炎症 & 免疫学

Biochem/physiol Actions

该抗体与非还原性血小板膜凝胶上的25 kDa分子量条带反应，并从碘125标记的血小板中免疫沉淀出类似的条带。该抗原在嗜酸粒细胞，粒细胞，单核细胞和许多基质细胞上表达。该CD9抗原属于细胞表面蛋白的TM4超家族，其N端和C端位于细胞质中。

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。

Immunogen

人血小板糖蛋白

Other Notes

浓度：请参考批次特异性浓缩物的检验报告。

Physical form

单克隆抗体以100μg/1ml溶于含有10 mM叠氮化钠和1 mg/ml牛血清白蛋白的磷酸盐缓冲液中。 我们建议每个实验室确定在其特定应用中使用的最佳工作滴定度。
形式：纯化
纯化的蛋白 A

Preparation Note

自发货之日起在4°C下可保存1年

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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存储类别

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

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Dmitry Ter-Ovanesyan et al.
eLife, 10 (2021-11-17)
Extracellular vesicles (EVs) are released by all cells into biofluids and hold great promise as reservoirs of disease biomarkers. One of the main challenges in studying EVs is a lack of methods to quantify EVs that are sensitive enough and
V Zvereff et al.
British journal of cancer, 97(7), 941-948 (2007-09-13)
CD9, a member of the tetraspanin family of proteins, is involved in a variety of cellular interactions with many other proteins and molecules. Although CD9 has been implicated in cell fusion, migration and cancer progression, the detailed function of this
Yesim Verel-Yilmaz et al.
Frontiers in cell and developmental biology, 9, 697939-697939 (2021-08-10)
Due to a grim prognosis, there is an urgent need to detect pancreatic ductal adenocarcinoma (PDAC) prior to metastasis. However, reliable diagnostic imaging methods or biomarkers for PDAC or its precursor lesions are still scarce. ADAM8, a metalloprotease-disintegrin, is highly
Yuan-Yin Chen et al.
Cancers, 13(21) (2021-11-14)
C-Circles, self-primed telomeric C-strand templates for rolling circle amplification, are the only known alternative-lengthening-of-telomeres (ALT)-specific molecule. However, little is known about the biology of C-Circles and if they may be clinically useful. Here we show that C-Circles are secreted by
Xiaoman Zhang et al.
PloS one, 17(6), e0270634-e0270634 (2022-06-25)
Extracellular vesicles (EVs) have attracted much attention as potential diagnostic biomarkers for human diseases. Although both plasma and serum are utilized as a source of blood EVs, it remains unclear whether, how and to what extent the choice of plasma
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