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Merck
CN

SAB4200127

Sigma-Aldrich

Anti-DYX1C1 antibody produced in rabbit

enhanced validation

~1.5 mg/mL, affinity isolated antibody

别名:

Anti-DYX1, Anti-DYXC1, Anti-Dyslexia susceptibility 1 candidate 1, Anti-EKN1, Anti-FLJ37882, Anti-MGC70618, Anti-RD

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关于此项目

UNSPSC代码:
12352203
NACRES:
NA.41
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生物来源

rabbit

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

表单

buffered aqueous solution

分子量

antigen ~48 kDa

种属反应性

human

包装

antibody small pack of 25 μL

增强验证

recombinant expression
Learn more about Antibody Enhanced Validation

浓度

~1.5 mg/mL

技术

western blot: 1-2 μg/mL using HEK-293T cell lysate expressing human DYX1C1

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... DYX1C1(161582)
mouse ... Dyx1c1(67685)
rat ... Dyx1c1(363096)

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一般描述

The dyslexia susceptibility 1 candidate 1 (DYX1C1) gene is located near the DYX1 locus in the human chromosome 15q21. The encoded protein contains three tetratricopeptide repeat (TPR) domains. DYX1C1 is expressed in several tissues, including the brain, lungs and kidney. The protein resides in the nucleus of the cortical neurons and glial cells.

应用

Anti-DYX1C1 antibody produced in rabbit is suitable for immunoblotting.

生化/生理作用

Anti-DYX1C1 specifically recognizes human DYX1C1.
The dyslexia susceptibility 1 candidate 1 (DYX1C1) gene is identified as a candidate gene implicated in dyslexia due to chromosomal translocations. The encoded protein is involved in neuronal migration and other developmental processes. It also functions as protein interaction modules. Knockdown of the gene DYX1C1 by RNA interference (RNAi) in rats causes a deficit in neuronal migration in the developing neocortex, auditory processing, and spatial learning, supporting the role of DYX1C1 in dyslexia. The protein is known to be implicated as a cancer biomarker in colorectal cancer.

外形

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

制备说明

For continuous use, store at 2–8 °C for up to one month. For extended storage, freeze in working aliquots at –20 °C. Repeated freezing and thawing is not recommended. Storage in “frost-free” freezers is also not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.

免责声明

Unless otherwise stated in our catalog, our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

10 - Combustible liquids

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品
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分析证书(COA)

Lot/Batch Number

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Albert M Galaburda et al.
Nature neuroscience, 9(10), 1213-1217 (2006-09-27)
All four genes thus far linked to developmental dyslexia participate in brain development, and abnormalities in brain development are increasingly reported in dyslexia. Comparable abnormalities induced in young rodent brains cause auditory and cognitive deficits, underscoring the potential relevance of
Mikko Taipale et al.
Proceedings of the National Academy of Sciences of the United States of America, 100(20), 11553-11558 (2003-09-05)
Approximately 3-10% of people have specific difficulties in reading, despite adequate intelligence, education, and social environment. We report here the characterization of a gene, DYX1C1 near the DYX1 locus in chromosome 15q21, that is disrupted by a translocation t(2;15)(q11;q21) segregating
Yun-Ji Kim et al.
Journal of cancer research and clinical oncology, 135(2), 265-270 (2008-07-12)
DYX1C1 has three alternatively spliced transcripts. Therefore, we expect that alternative transcripts of DYX1C1 are used as a biomarker to detect specific cancer. RT-PCR analysis is conducted in order to detect expression of the DYX1C1 gene and the PCR products
Steven W Threlkeld et al.
Brain research bulletin, 71(5), 508-514 (2007-01-30)
Developmental malformations of cortex have been shown to co-occur with language, learning, and other cognitive deficits in humans. Rodent models have repeatedly shown that animals with such developmental malformations have deficits related to auditory processing and learning. More specifically, freeze-lesion

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