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Merck
CN

AB9908

抗-QKI-7 抗体

serum, Chemicon®

别名:

Quaking Protein

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
polyclonal
Application:
immunoprecipitation (IP)
western blot
Species reactivity:
mouse, rat, human
Citations:
9
Technique(s):
immunoprecipitation (IP): suitable
western blot: suitable
Uniprot accession no.:
Q96PU8

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产品名称

抗-QKI-7 抗体, serum, Chemicon®

biological source

rabbit

conjugate

unconjugated

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

mouse, rat, human

manufacturer/tradename

Chemicon®

technique(s)

immunoprecipitation (IP): suitable
western blot: suitable

NCBI accession no.

NM_006775.1
NM_206853.1
NM_206854.1
NM_206855.1

UniProt accession no.

Q96PU8

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

100

Gene Information

human ... QKI(9444)

相关类别

Analysis Note

对照
阳性对照：神经胶质细胞、星形胶质细胞和少突胶质细胞

Application

抗-QKI-7抗体是针对QKI-7的抗体，可用于IP & WB。
研究子类别
发育神经科学

RNA结合蛋白（RBP）
研究类别
神经科学

Biochem/physiol Actions

QKI-7 （Quaking 蛋白）该抗体识别~42 kDa蛋白。

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

QKI 是一种RNA结合蛋白，在髓鞘形成中起主导作用。通过调节pre-mRNA剪接、mRNA输出、mRNA稳定性和蛋白质翻译起作用。它通过可变剪接调节。

Immunogen

来自小鼠QKI-7的合成肽。

Physical form

液体。
血清

Preparation Note

自收到之日起，在 -20&deg:C 以未稀释的等分试样可保存 12 个月。应避免反复冻/融循环。

Legal Information

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

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存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Valerie Bríd O'Leary et al.
Oncotarget, 8(45), 78397-78409 (2017-11-08)
Generated by Quaking (QKI), circular RNAs (circRNAs) are newly recognised non-coding RNA (ncRNA) members characterised by tissue specificity, increased stability and enrichment within exosomes. Studies have shown that ionizing radiation (IR) can influence ncRNA transcription. However, it is unknown whether
Ruben G de Bruin et al.
Epigenomes, 4(1) (2020-02-13)
In the pathophysiologic setting of acute and chronic kidney injury, the excessive activation and recruitment of blood-borne monocytes prompts their differentiation into inflammatory macrophages, a process that leads to progressive glomerulosclerosis and interstitial fibrosis. Importantly, this differentiation of monocytes into
Hiroaki Hojo et al.
The Journal of biological chemistry, 295(2), 390-402 (2019-12-04)
MicroRNA-122 (miR-122) is highly expressed in hepatocytes, where it plays an important role in regulating cholesterol and fatty acid metabolism, and it is also a host factor required for hepatitis C virus replication. miR-122 is selectively stabilized by 3' adenylation
Zhejia Zhang et al.
Oncology letters, 15(4), 5841-5848 (2018-03-21)
Thyroid cancer is the most frequently occurring type of endocrine tumor, with a rapidly increasing incidence rate. MicroRNA (miR)-574-5p is a candidate oncogene in various types of cancer. The present study identified that miR-574-5p affected the cell cycle distribution and
Ruben G de Bruin et al.
Nature communications, 7, 10846-10846 (2016-04-01)
A hallmark of inflammatory diseases is the excessive recruitment and influx of monocytes to sites of tissue damage and their ensuing differentiation into macrophages. Numerous stimuli are known to induce transcriptional changes associated with macrophage phenotype, but posttranscriptional control of
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相关内容

RNA-Binding Protein Immunoprecipitation

All eukaryotic organisms require tight regulation of gene expression for complex processes such as development, differentiation, cell specification, and responses to environmental stimuli. Many genes are regulated post-transcriptionally, in addition to transcriptional mechanisms of gene regulation. RNA-binding proteins (RBPs) are essential for post-transcriptional gene regulation, linking transcription and translation in many processes including transcription, splicing, export, rate of translation and turnover. In all of these events, RBPs coordinate regulation of the amount of protein produced from mRNA transcripts.

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