CELLection™ Pan Mouse IgG Kit
Invitrogen™

CELLection™ Pan Mouse IgG Kit

このキットとマウスIgGを使用し、マウス以外のすべての種から細胞集団をポジティブ単離します。抗体は、DNAリンカーを介してCELLection™ Dynabeads™の表面に結合します。このリンカーは切断可能な部位を提供するため、単離後に細胞からビーズを放出および除去できます。ビーズフリーの細胞は生存可能で、あらゆる下流アプリケーションで使用できます。このキットの内容:ヒト抗マウスIgGモノクローナルでコーティングされたCELLection™詳細を見る
製品番号(カタログ番号)数量
11531D5 mL
製品番号(カタログ番号) 11531D
価格(JPY)
-
数量:
5 mL
このキットとマウスIgGを使用し、マウス以外のすべての種から細胞集団をポジティブ単離します。抗体は、DNAリンカーを介してCELLection™ Dynabeads™の表面に結合します。このリンカーは切断可能な部位を提供するため、単離後に細胞からビーズを放出および除去できます。ビーズフリーの細胞は生存可能で、あらゆる下流アプリケーションで使用できます。

このキットの内容:ヒト抗マウスIgGモノクローナルでコーティングされたCELLection™ Dynabeads™、およびDNAseリリースバッファー

アプリケーション:

• 任意のマウスIgGを使用し、あらゆる種(マウスを除く)の細胞をポジティブ単離および剥離
• フローサイトメトリー、細胞培養、およびすべての細胞ベースアッセイに対応
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
抗体フラグメント全抗体
細胞タイプマウス以外のすべての種のすべての細胞
染色剤タイプCELLection™ Pan
宿主種マウス
単離技術ポジティブ単離
セル数合計で約2x10^9個の細胞を処理可能
出力実行可能性≧95%
製品ラインCELLection、Dynabeads
純度または品質グレード研究グレード
数量5 mL
反応性マウス以外のすべての種
サンプルタイプPBMC、組織消化物、血液
出荷条件室温
出発物質セル番号1つの単離あたり1 x 10^7個のPBMC
ターゲット種マウス以外のすべての種
製品タイプ抗体コーティングビーズ
Unit SizeEach
組成および保存条件
冷蔵庫(2~8℃)に保存。

よくあるご質問(FAQ)

When isolating cells with Dynabeads magnetic beads, what is more important: bead-to-target cell ratio or the concentration of beads in the bead/cell mixture?

Both bead-to-target cell ratio and the concentration of beads in the bead/cell mixture are important and should be considered. For example, when using the Dynabeads magnetic beads M-450 CD4 positive isolation or depletion kit, a 4:1 bead-to-target cell ratio should be maintained. To capture 95% of target cells for molecular applications, the bead concentration must always be 1 x 10e7 beads per milliliter of sample. To deplete 99% CD4 cells from the starting sample, the bead concentration must always be 2 x 10e7 beads per milliliter of sample. Please consult the package insert for recommended bead concentrations of each product.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Will Dynabeads magnetic beads be internalized if cultured with the beads on?

Whether cells will internalize the Dynabeads magnetic beads during culture will depend on the cell type. Due to the bead size (usually 4.5µm in diameter) Dynabeads magnetic beads will not be internalized into the endocytic pathway e.g., via clathrin coated pits. The clathrin coated pits are typically not more than 500 nm in size, which is far too small for endocytosis of the beads. However, if cells with phagocytic activities (e.g., monocytes/macrophages) are present, the Dynabeads magnetic beads will be phagocytosed into the phagolysosomes by these specialized cells. So it would really depend on the cell type.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Is there a method to remove the Dynabeads magnetic beads from isolated cells if the bead releasing reagent is not available?

We offer several Dynabeads magnetic beads that can be used for either positive isolation (keep the target cells) or for depletion (remove the target cell from a sample) that does not include any release mechanism:

- Dynabeads magnetic beads for depletion: Using Dynabeads magnetic beads for depletion is a very fast, efficient and easy method. Use pre-coated Dynabeads magnetic beads or coat your own target antibody onto our secondary coated beads, add to any sample (e.g., whole blood, PBMC, buffy coat, tissue digests), incubate for 20 minutes with mixing, apply to a magnet for 2 minutes, and you have your cells depleted.

- Dynabeads magnetic beads for positive isolation for molecular downstream assays: Positive isolation of target cells without bead release can be used when the aim is downstream molecular studies such as DNA, RNA, or protein analysis. In these applications, the isolated cells can be lysed while the beads are attached to the cells, and the beads can be removed after cell lysis. If the bead presence is not a problem, you can also culture the cells with the beads on. In most cases the surface antigen will be internalized after 2-3 days, and then the beads will fall off since the beads are too big to be internalized by the endocytosis pathway.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Will Dynabeads magnetic beads be internalized by the target cells?

In general, the size of the Dynabeads magnetic beads is so large that they will not be internalized. The clathrin-coated pits are typically not more than 500 nm in size, which will be too small for Dynabeads magnetic beads to be internalized by endocytosis. However, if the target cells have phagocytic activities such as monocytes/macrophages, the Dynabeads magnetic beads could be internalized by phagocytosis.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

How do Dynabeads CELLection cell isolation kits work?

The CELLection kits contain Dynabeads magnetic beads coated with a DNA linker (either via streptavidin or via an antibody for cell isolation) and a DNase enzyme for bead release. After the beads capture the target cells (either directly or indirectly), the cells are released by DNAse treatment to cleave the linker. As a result, the target cells are released from the Dynabeads magnetic beads, but still linked with capture antibody.

We offer three Dynabeads CELLection cell isolation kits:

- CELLection Epithelial Enrich Kit (Cat. No. 16203) contains Dynabeads magnetic beads coupled with anti-EpCAM monoclonal antibody
- CELLection Biotin Binder Kit (Cat. No. 11533D) is used for positive isolation of target cells with your own biotinylated antibody
- CELLection Pan Mouse IgG Kit (Cat. No. 11531D) is used for isolation of target cells with your own mouse IgGs

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

引用および参考文献 (5)

引用および参考文献
Abstract
The postnatal rat aorta contains pericyte progenitor cells that form spheroidal colonies in suspension culture.
Authors:Howson KM, Aplin AC, Gelati M, Alessandri G, Parati EA, Nicosia RF,
Journal:Am J Physiol Cell Physiol
PubMed ID:16079185
'Pericytes play an important role in modulating angiogenesis, but the origin of these cells is poorly understood. To evaluate whether the mature vessel wall contains pericyte progenitor cells, nonendothelial mesenchymal cells isolated from the rat aorta were cultured in a serum-free medium optimized for stem cells. This method led to ... More
p27Kip1 and cyclin D1 are necessary for focal adhesion kinase regulation of cell cycle progression in glioblastoma cells propagated in vitro and in vivo in the scid mouse brain.
Authors:Ding Q, Grammer JR, Nelson MA, Guan JL, Stewart JE, Gladson CL,
Journal:J Biol Chem
PubMed ID:15557280
'We have reported previously that the expression of focal adhesion kinase (FAK) is elevated in glioblastomas and that expression of FAK promotes the proliferation of glioblastoma cells propagated in either soft agar or in the C.B.17 severe combined immunodeficiency (scid) mouse brain. We therefore determined the effect of FAK on ... More
D-4F induces heme oxygenase-1 and extracellular superoxide dismutase, decreases endothelial cell sloughing, and improves vascular reactivity in rat model of diabetes.
Authors:Kruger AL, Peterson S, Turkseven S, Kaminski PM, Zhang FF, Quan S, Wolin MS, Abraham NG,
Journal:Circulation
PubMed ID:15939814
'BACKGROUND: Apolipoprotein A1 mimetic peptide, synthesized from D-amino acid (D-4F), enhances the ability of HDL to protect LDL against oxidation in atherosclerotic animals. METHODS AND RESULTS: We investigated the mechanisms by which D-4F provides antioxidant effects in a diabetic model. Sprague-Dawley rats developed diabetes with administration of streptozotocin (STZ). We ... More
CD31 promotes beta1 integrin-dependent engulfment of apoptotic Jurkat T lymphocytes opsonized for phagocytosis by fibronectin.
Authors:Vernon-Wilson EF, Auradé F, Brown SB,
Journal:J Leukoc Biol
PubMed ID:16551678
Phagocyte integrins, by binding "bridging" molecules, mediate the ingestion of late apoptotic cells and apoptotic bodies by mechanisms that remain obscure. We recently reported that human monocyte-derived macrophages capture viable and apoptotic human leukocytes through homophilic interactions involving CD31 and that CD31 then promotes the engulfment of apoptotic cells or ... More
Epstein-Barr virus infection of Langerhans cell precursors as a mechanism of oral epithelial entry, persistence, and reactivation.
Authors:Walling DM, Ray AJ, Nichols JE, Flaitz CM, Nichols CM,
Journal:J Virol
PubMed ID:17376908
Epstein-Barr virus (EBV) is a ubiquitous human herpesvirus associated with many malignant and nonmalignant human diseases. Life-long latent EBV persistence occurs in blood-borne B lymphocytes, while EBV intermittently productively replicates in mucosal epithelia. Although several models have previously been proposed, the mechanism of EBV transition between these two reservoirs of ... More