Name: flash freezing and cryosectioning e12.5 mouse brain
Uploaded: 2007-05-28T00:00:00
Description: Watch this Scientific Journal Video about Flash Freezing and Cryosectioning E12.5 Mouse Brain at JoVE.com

<ol><li>希望の時間のためのPBS中4％パラホルムアルデヒドで細胞を固定してください。 </li><li>スクロース注入組織（cryoprotection） <ol><li> 2059チューブにPBS w / vの30％ショ糖液を作る。 </li><li> PBSの組織が3倍リンス（ロッキング付き〜5分）。 </li><li> 30％ショ糖溶液中で組織を置きます。組織は、シンクしません。 </li><li> ℃で一晩、または、それが沈没するまで4で組織を置きます。 </li></ol></li><li>情報と方向でcryom...

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		<th>Material Name</th>
		<th>Type</th>
		<th>Company</th>
		<th>Catalogue Number</th>
		<th>Comment</th>
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<td>Tissue-Tek Cryomold</td>
<td>&nbsp;</td>
<td>Ted Pella, Inc.</td>
<td>27181</td>
<td>&nbsp;</td>
<tr>
<td>O.C.T.</td>
<td>&nbsp;</td>
<td>Ted Pella, Inc</td>
<td>27050</td>
<td>&nbsp;</td>
<tr>
<td>Sucrose solution</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>30% sucrose solution in PBS w/v</td>
</tr>
<tr>
<td>paraformaldehyde</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>4% paraformaldehyde in PBS </td>
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flash freezing and cryosectioning e12.5 mouse brain

Watch this Scientific Journal Video about Flash Freezing and Cryosectioning E12.5 Mouse Brain at JoVE.com

Flash Freezing and Cryosectioning E12.5 Mouse Brain

<p class="jove_content">このビデオで明らかに瞬間冷凍のためのテクニックであり、マウスの胚脳組織をセクショニング。クリオスタットを使用するための有用なヒントが得られる組織のセクションは、クラックや他の歪みのないことを保証するために削減しながら使用できるトラブルシューティングの方法を含めて、与えられている。</p>

Flashは、E12.5マウス脳の凍結とCryosectioning

Research

JoVE Journal

Biology

Freezing Human ES Cells

凍結ヒトES細胞

Here we demonstrate how our lab freezes HuES human embryonic stem cell lines.  A healthy, exponentially expanding culture is washed with PBS to remove ...

Freezing, Thawing, and Packaging Cells for Transport

トランスポートのための凍結、融解、およびパッケージング細胞

Cultured mammalian cells are used extensively in cell biology studies. It requires a number of special skills in order to be able to preserve the ...

Freezing and Thawing Human Embryonic Stem Cells

ヒト胚性幹細胞を凍結融解

Since James Thomson et al developed a technique in 1998 to isolate and grow hES in culture, freezing cells for later use and thawing and expanding cells ...

<em>In vivo</em> Imaging and Therapeutic Treatments in an Orthotopic Mouse Model of Ovarian Cancer

In vivo Imaging and Therapeutic Treatments in an Orthotopic Mouse Model of Ovarian Cancer

<em>生体</em>イメージングおよび卵巣癌の同所性マウスモデルにおける治療的処置<em>の</em>

Human cancer and response to therapy is better represented in orthotopic animal models.  This paper describes the development of an orthotopic mouse model ...

ReAsH/FlAsH Labeling and Image Analysis of Tetracysteine Sensor Proteins in Cells

ReAsH /フラッシュラベルと細胞におけるテトラセンサータンパク質の画像解析

Fluorescent proteins and dyes are essential tools for the study of protein trafficking, localization and function in cells.  While fluorescent 
proteins ...

Cryosectioning Yeast Communities for Examining Fluorescence Patterns

蛍光パターンを調査するための凍結セクショニング酵母コミュニティ

Microbes typically live  in communities. The spatial organization  of cells within a community is believed to impact the survival and function of the  ...

Tissue Triage and Freezing for Models of Skeletal Muscle Disease

組織トリアージや骨格筋疾患のモデルのために凍結

Skeletal muscle is a unique tissue because of its structure and function, which requires specific protocols for tissue collection to obtain optimal ...

Cryosectioning Method for Microdissection of Murine Colonic Mucosa

マウス結腸粘膜の顕微解剖のための凍結切片法

The colonic mucosal tissue provides a vital barrier to luminal antigens. This barrier is composed of a monolayer of simple columnar epithelial cells. The ...

Cryosectioning of Contiguous Regions of a Single Mouse Skeletal Muscle for Gene Expression and Histological Analyses

遺伝子発現と組織学的分析のためにシングルマウス骨格筋の連続領域の凍結切片化

With this method, consecutive cryosections are collected to enable both microscopy applications for tissue histology and enrichment of RNA for gene ...

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy

フラッシュとフリーズ：電子顕微鏡でメンブレンダイナミクスをキャプチャするために新しい技術

Cells constantly change their membrane architecture and protein distribution, but it is extremely difficult to visualize these events at a temporal and ...