MYEOV/IGH融合基因t(11;14)探針

 廣州健侖生物科技?有限公司 

本司長期供應(yīng)尼古?。商鎸帲z測試劑盒，其主要品牌包括美國NovaBios、廣州健侖、廣州創(chuàng)侖等進(jìn)口產(chǎn)品，國產(chǎn)產(chǎn)品，試劑盒的實驗方法是膠體金方法。

我司還有很多熒光原位雜交系列檢測試劑盒以及各種FISH基因探針和染色體探針等，。

MYEOV/IGH融合基因t(11;14)探針

   本試劑盒主要用于MYEOV/IGH融合基因t(11;14)的檢測，里面包括即用型雜交液和DAPI復(fù)染劑。
本試劑盒僅供科研使用。

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MYEOV/IGH融合基因t(11;14)探針

二維碼掃一掃

【公司名稱】 廣州健侖生物科技有限公司
【】    楊永漢 

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【騰訊 】
【公司地址】 廣州清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號二期2幢101-3室

【企業(yè)文化宣傳】MYEOV/IGH融合基因t(11;14)探針

Most of the pancreas (95%) consists of two exocrine cells: acinus and ductal cells. Acinar cells produce digestive enzymes, catheter cells secrete bicarbonate, and transport digestive enzymes to the intestinal channel. The remaining 5% of the pancreas is the islet, dispersed in exocrine tissues and ducts, and contains endocrine cells that secrete hormones that maintain stable blood sugar. Islets contain five types of endocrine cells, alpha cells, beta cells, delta cells, gamma cells and epsilon cells.
This study uses large-scale single-cell sequencing method of droplet based on the principle of drawing the human and mouse more than 12000 transcription pancreatic cells provide a reference spectrum; a new cell type specific transcription factor, signal receptor and treatment related genes for the subsequent discovery.
research method
2.1 droplet platforms were used to separate 2000 pancreatic cells from 4 individuals, 10000 and 2 mice, and 12000 cells were subjected to single cell transcriptome sequencing, with 100 thousand reads per cell. The human pancreas cells came from 4 donors, and the mice's pancreatic cells came from 2 mice.

2.2 immunohistochemical study: FFAR4/GPR120, MUC1 and CFTR.

experimental result

3.1 single cell sequencing identification of subgroups of expression profiles of pancreatic cell types

After filtration, 12000 cells contained 8629 cells from 4 individuals, and 1886 from each mouse cell, with approximay 6000 transcripts and 2000 genes. By cluster analysis, human and mice were divided into 14 and 13 subgroups, and the characteristic genes of each subgroup were displayed.

The relationship between the 3.2 cell subtypes explains the consistent type of cell type between human and mouse strains

Analyzing all the cell types detected in humans and mice, we found almost the same pattern of cell relationships in humans and mice.

In addition, the consistency of cell types between the same species was analyzed. Compared with human 1 and 3 of human ductal cells, the correlation coefficient R2=0.92 was much higher than that of the same donor. The correlation coefficient R2=0.72 of different cell types of the same donor showed that the average transcription of cell type was conservative.

3.3 endocrine specific gene expression

The sequencing data also provides a treasure house for the study of gene expression. For example, FFAR4 related to drug development, UCN3 related to functional maturity of beta cells, LEPR related to genetic related DLK1, and mouse model of human disease
FFAR4/GPR120 agonists are now being developed to treat diabetes, because they play the role of insulin, which can reduce blood sugar. The study found that beta cells and human delta cell FFAR4 gene expression at the same time, in order to further verify, then we on the islet for immunohistochemical staining, found confirmed the presence of FFAR4 in these two cells, the overthrow of the thought that FFAR4 only exists in the delta cell in conclusion.

膵臓のほとんど（95）は二つの外分泌細(xì)胞：腺泡やカテーテル細(xì)胞。腺泡細(xì)胞が消化酵素、カテーテル細(xì)胞碳酸氫鹽分泌し、輸送、消化酵素腸までチャネル。膵臓の殘りの5 %は膵島、分散外分泌組織やカテーテル內(nèi)分泌、血糖の安定維持を含めたホルモンの內(nèi)分泌細(xì)胞。膵島含め5種類の內(nèi)分泌細(xì)胞のタイプ、α細(xì)胞、β細(xì)胞、δ細(xì)胞、γ細(xì)胞やε細(xì)胞。
本研究で使用するにもとづいて液滴の原理の大規(guī)模な単細(xì)胞の転寫組シークエンシング方法、描く人とマウスじゅうに、000以上の膵臓細(xì)胞の転寫譜；後続新しい発見の細(xì)胞のタイプ、特異性の転寫因子、信號受容體や治療に関する?yún)⒖歼z伝子。
研究方法
2 . 1液滴プラットフォーム、分離よんしよ個人じゅう、000とにマウスのだけに、000膵臓細(xì)胞、共じゅうに、000細(xì)胞を単細(xì)胞の転寫組シークエンシング、すべての細(xì)胞じゅう萬reads數(shù)。その中の人のすい臓細(xì)胞は4人のドナー、マウスのすい臓細(xì)胞から2つのマウスの品系から來た。

2 . 2免疫組化研究：FFAR4 / GPR120、MUC1 and CFTR。

実験の結(jié)果

3 . 1単細(xì)胞シークエンシング鑑定した膵臓細(xì)胞のタイプの発現(xiàn)プロファイル亜群

じゅうに、000個もの細(xì)胞を含めたはちろ過後、629個もの細(xì)胞からよんしよいち個人や、886から約ろくマウス細(xì)胞、000本、2000個遺伝子転寫。人とネズミをそれぞれ14と13の亜群に分け、それぞれの亜群の特徴的な遺伝子を展示した

3 . 2細(xì)胞亜型の間の関係を説明した人とマウス品係の間に一緻の細(xì)胞のタイプ

人とネズミの上で検出したすべての細(xì)胞のタイプを分析して、私たちは人とネズミの上でほとんど同じ細(xì)胞関係モード図を発見しました。

また、分析と同じ種個體間の細(xì)胞のタイプの整合性を比較した人と人がいちさんのカテーテル細(xì)胞、関連係數(shù)R 2 = 0 .上回る同ドナーと細(xì)胞のタイプの関連係數(shù)R 2 = 0 . 72を表明し、細(xì)胞のタイプの平均転寫保守的な

3.3內(nèi)分泌性遺伝子表現(xiàn)

シークエンシングデータも提供した研究遺伝子発現(xiàn)の寶庫。たとえばと薬物の開発に関するFFAR4、β細(xì)胞の機(jī)能と成熟し、関連のUCN3と遺伝相関のDLK1、人類の疾病のモデルマウスに関するLEPR
FFAR4 / GPR120の興奮剤に対して現(xiàn)在開発中の糖尿病の治療に使用、彼らを発揮しているようにインスリンの作用、血糖値を下げる。本研究発見人類のβ細(xì)胞や遺伝子を同時に表現(xiàn)FFAR4δ細(xì)胞、さらに次のために検証し、私たちは膵島を免疫組化染色、発見FFAR4存在確認(rèn)はこの2種類の細(xì)胞で滅亡、前に思うしか存在しFFAR4δ細(xì)胞の中の結(jié)論。