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Merck

APOAF

アネキシンV-FITCアポトーシス検出キット

別名:

Annexin V-FITC, Apoptosis probe FITC

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この商品について

NACRES:
NA.84
UNSPSC Code:
12352207

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usage

(20 tests)

packaging

pkg of 1 kit

technique(s)

flow cytometry: suitable

application(s)

cell analysis
detection

detection method

fluorometric

shipped in

wet ice

storage temp.

2-8°C

Quality Level

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当該品目
APOACS7111QIA39
technique(s)

flow cytometry: suitable

technique(s)

flow cytometry: suitable

technique(s)

flow cytometry: suitable, immunocytochemistry: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable

technique(s)

flow cytometry: suitable

usage

(20 tests)

usage

sufficient for 200 tests

usage

-

usage

sufficient for 50 tests

packaging

pkg of 1 kit

packaging

pkg of 1 kit

packaging

-

packaging

-

application(s)

cell analysis
detection

application(s)

cell analysis
detection

application(s)

-

application(s)

-

detection method

fluorometric

detection method

fluorometric

detection method

fluorometric

detection method

fluorometric

shipped in

wet ice

shipped in

wet ice

shipped in

dry ice

shipped in

wet ice

Application

アネキシンV -FITCアポトーシス検出キットは、以下のことに使用されました:
  • 前立腺癌の治療における、G. lucidum抽出物の活性を測定するための、LNCaP前立腺癌細胞の染色。[1]
  • 前立腺腫瘍細胞におけるDBP-maf(ビタミン D 結合タンパク質-マクロファージ活性化因子)の阻害活性を研究するための、腫瘍細胞の標識化。[2]
  • フリッパーゼ活性の間接測定。[3]

Features and Benefits

TUNELのようなDNAベ-スの方法よりもプロセスの初期でアポト-シスを検出できます。
  • 細胞を迅速にラベリング。細胞染色はわずか10分。
  • 細胞の固定や処理の必要がなく、検出時間を短縮、細胞をさらに検討することも可能。
  • 2次染色用の色素として、キットにはヨウ化プロピジウムが用意されており、生存細胞およびネクロ-シス細胞と、アポト-シス細胞の区別が可能。

General description

アネキシンV-FITCキットは、アポトーシス細胞に結合したアネキシンVの蛍光検出や、フローサイトメトリーによる定量測定を可能にします。 アネキシンV-FITCキットでは、膜表面のホスファチジルセリンの位置を標識するために、フルオレセインイソチオシアネート(FITC)を結合させたアネキシンVを使用します。 本キットは、細胞膜が完全に無防備となっているネクローシス細胞中のDNAを標識するためのヨウ化プロピジウム(PI)を含みます。 この組み合わせにより、初期のアポトーシス細胞(アネキシンV陽性、PI陰性)、ネクローシス細胞(アネキシンV陽性、PI陽性)、および生細胞(アネキシンV陰性、PI陰性)を区別できます。

Other Notes

使用前に全てのコンポーネントを、室温に戻してください。

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詳細
価格

保管分類

10 - Combustible liquids


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Denise C Arruda et al.
The Journal of biological chemistry, 287(18), 14912-14922 (2012-02-16)
Complementarity-determining regions (CDRs) from monoclonal antibodies tested as synthetic peptides display anti-infective and antitumor activities, independent of the specificity of the native antibody. Previously, we have shown that the synthetic peptide C7H2, based on the heavy chain CDR 2 from
Monika Kallubai et al.
Journal of biomolecular structure & dynamics, 37(3), 623-640 (2018-01-30)
Our study focus on the biological importance of synthesized 5β-dihydrocortisol (Dhc) and 5β-dihydrocortisol acetate (DhcA) molecules, the cytotoxic study was performed on breast cancer cell line (MCF-7) normal human embryonic kidney cell line (HEK293), the IC50 values for MCF-7 cells
Jianzhong Li et al.
Scientific reports, 6, 23975-23975 (2016-04-08)
Metformin, one of the most common prescriptions for patients with type 2 diabetes, is reported to protect the kidney from gentamicin-induced nephrotoxicity. However, the role and mechanisms for metformin in preventing cisplatin-induced nephrotoxicity remains largely unknown. In this study, a
C Pigault et al.
Journal of molecular biology, 236(1), 199-208 (1994-02-11)
Annexins are intracellular proteins which bind to membranes in a Ca(2+)-dependent manner and which have been proposed to play regulatory roles in different membrane processes. In the present study, the stoichiometry of the Ca(2+)-dependent binding of annexin V to phosphatidylserine
Kalvin J Gregory et al.
PloS one, 5(10), e13428-e13428 (2010-10-27)
Vitamin D binding protein-macrophage activating factor (DBP-maf) is a potent inhibitor of tumor growth. Its activity, however, has been attributed to indirect mechanisms such as boosting the immune response by activating macrophages and inhibiting the blood vessel growth necessary for

資料

Cellular apoptosis assays to detect programmed cell death using Annexin V, Caspase and TUNEL DNA fragmentation assays.

Discover cell culture applications for hormones including insulin and dexamethasone. Explore high-quality supplements.

Quality control guidelines to maintain high quality authenticated and contamination-free cell cultures. Free ECACC handbook download.

質問

1–6/6 質問  
  1. When using Product APOAF, Annexin V-FITC Apoptosis Detection Kit, I have cells that are Annexin V FITC negative and PI positive.  What are these cells?

    1 回答
    1. It is not possible to have cells that are PI positive without the cells also being positive for Annexin V binding.  Cells are PI positive because the membrane has been compromised.  If this is the case, Annexin V can also enter the cell and bind to the PS on the internal cell membrane. The gating on the histogram for the FITC channel should be changed so that all cells that are PI positive are also Annexin V positive.

      役に立ちましたか?

  2. Can I use Product APOAF, Annexin V-FITC Apoptosis Detection Kit, to differentiate cells that are dead due to necrosis or apoptosis?

    1 回答
    1. When using a kinetic study (various time points), you can show the progression of the cells from viable (annexin V FITC negative, PI negative), to annexin FITC positive, PI negative (membrane flip) to annexin V FITC positive, PI positive (dead).  If there are cells that are double positive when starting, it is not possible to guarantee that the cell death occurred due to apoptosis with this assay.

      役に立ちましたか?

  3. What is the Department of Transportation shipping information for this product?

    1 回答
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

      役に立ちましたか?

  4. Can Product APOAF, Annexin V-FITC Apoptosis Detection Kit be used on fixed cells?

    1 回答
    1. No. Product APOAF, Annexin V-FITC Apoptosis Detection Kit must be performed on live cells in order to measure Apoptosis. The assay is based on the externization of phosphatidylserine from the inner cell membrane to the outer cell membrane.  If the membrane is preturbed due to fixation, non-speciifc staining of the inner cell membrane might occur

      役に立ちましたか?

  5. When using the Annexin V-FITC Apoptosis Detection Kit, Product APOAF, can I use any buffer for resuspending my cells?

    1 回答
    1. The binding buffer included in the kit needs to be used for resuspending cells.  The buffer contains calcium chloride at a final (1X) concentration of 2.5 mM which is necessary for the binding of annexin V to phosphatidylserine.

      役に立ちましたか?

  6. What wavelength do I use to detect Annexin V-FITC and Propidium Iodide when using Annexin V-FITC Apoptosis Detection Kit, Product APOAF?

    1 回答
    1. Annexin V FITC will have a maximum emission of 528 nm. This can be measured in the standard FITC Channel on a flow cytometer (FL1).  Propidium Iodide has a maximum emission of 620 nm.  This is measured on the short red channel on a flow cytometer (FL2 or FL3).

      役に立ちましたか?

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