Monkey (cynomolgus) Cryopreserved Hepatocytes, Plateable Male
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Gibco™

Monkey (cynomolgus) Cryopreserved Hepatocytes, Plateable Male

これらの播種可能凍結保存オスカニクイザル肝細胞は、一般的な第I相および第II相薬物代謝酵素活性を特性として備えています。バイアルあたりの細胞数:400~800万個GIBCO肝細胞で必要な結果を得られます高い生存率、適切な細胞形態、代謝活性を備えた高品質の肝細胞は、in vitro⁄in vivoの相関関係を引き出し、化合物の運命に関して適切な決定を下す能力を高めます。経験豊富な技術者と当社独自の単離技術を厳格なリリース仕様と組み合わせることで詳細を見る
製品番号(カタログ番号)数量
MKCP101バイアル
製品番号(カタログ番号) MKCP10
価格(JPY)
-
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数量:
1バイアル
これらの播種可能凍結保存オスカニクイザル肝細胞は、一般的な第I相および第II相薬物代謝酵素活性を特性として備えています。

バイアルあたりの細胞数:400~800万個

GIBCO肝細胞で必要な結果を得られます
高い生存率、適切な細胞形態、代謝活性を備えた高品質の肝細胞は、in vitro⁄in vivoの相関関係を引き出し、化合物の運命に関して適切な決定を下す能力を高めます。経験豊富な技術者と当社独自の単離技術を厳格なリリース仕様と組み合わせることで、最高品質の凍結保存肝細胞を確実にお届けします。

各ロットは次の試験が行われています。
• 75%以上の生存率
• 付着の効率性
• 単層の形成と完全性
• 5日目のコンフルエンシーが80%以上
• 第I相および第II相酵素活性

関連リンク:

当社の凍結保存肝細胞の詳細を見る
当社の肝細胞全製品ラインを見る

注:
これらの製品にはLN2蒸気デュワーでの輸送が必要なため、追加料金が適用される場合があります。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
ドナー源シングルドナー
セル数4~8 x 10^6
製品ラインGibco
製品タイプ肝細胞
数量1バイアル
細胞タイプ肝実質細胞
形状凍結保存済み
性別オス
サル
Unit SizeEach
組成および保存条件
クライオストレージデュワーまたは-135℃のフリーザーに保存してください。

よくあるご質問(FAQ)

Who can I call if I have technical questions regarding cryopreserved hepatocytes?

Thermo Fisher Scientific has a dedicated team to answer questions regarding hepatocytes. You can send a question by email (hepaticproducts@thermofisher.com) or contact us by phone: US toll-free: (866) 952 3559

With my hepatocytes, I'm seeing rounding up of the cells, cellular debris, and/or holes in the monolayer, indicating dying cells. What should I do?

This could be due to the toxicity of the test compound. Here are other potential causes and recommendations:

-Sub-optimal culture medium: Use Williams Medium E with Plating and Incubation Supplement Packs; refer to our plating protocol
-Hepatocyte lot not characterized as plateable: Check lot specifications to ensure it is qualified for plating
-Cells were cultured for too long: In general, plateable cryopreserved hepatocytes should not be cultured for more than five days

I'm getting unexpected induction results with my hepatocytes. What could be causing this?

First of all, we recommend comparing results to those reported on our lot-specific characterization specification sheet (human cells) and also referring to our enzyme induction protocol. Here are other potential causes and recommendations:

-Sub-optimal monolayer confluency: Please see our recommendations for 'I have a sub-optimal monolayer confluency for my hepatocytes. What should I do?'
-Poor monolayer integrity: Please see our recommendations for 'With my hepatocytes, I’m seeing rounding up of the cells, cellular debris, and/or holes in the monolayer, indicating dying cells. What should I do?'
-Inappropriate positive control: Check positive control to ensure suitability
-Incorrect concentration of positive control: Use the correct concentration of positive control

I'm seeing sub-optimal bile canlicular formation with my hepatocytes. What should I do?

Please see the following causes and recommendations:

-Hepatocyte lot not transporter-qualified: Check lot specifications to ensure it is transporter-qualified
-Sub-optimal culture medium: Use Williams Medium E with Plating and Incubation Supplement Packs; refer to our plating protocol
-Not enough time for bile canaliculi to form: In general, at least 4-5 days in culture is required for bile canalicular network formation

I'm getting a loss of membrane integrity or cuboidal cell shape with my hepatocytes. What should I do?

Please see the following causes and recommendations:

-Hepatocyte lot not characterized as plateable: Check lot specifications to ensure it is qualified for plating
-Sub-optimal culture medium: Use Williams Medium E with Plating and Incubation Supplement Packs; refer to our plating protocol
-Cells were cultured for too long: In general, plateable cryopreserved hepatocytes should not be cultured for more than five days