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Merck

APOAF

Annexin V-FITC 凋亡检测试剂盒

别名:

Annexin V-FITC, Apoptosis probe FITC

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20 TEST

$443.00

$443.00


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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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APOACFITC1SBR00028
technique(s)

flow cytometry: suitable

technique(s)

flow cytometry: suitable

technique(s)

-

technique(s)

-

usage

(20 tests)

usage

sufficient for 200 tests

usage

-

usage

-

packaging

pkg of 1 kit

packaging

pkg of 1 kit

packaging

pkg of (Kit contains reagents for 5 conjugations.)

packaging

-

application(s)

cell analysis
detection

application(s)

cell analysis
detection

application(s)

-

application(s)

-

detection method

fluorometric

detection method

fluorometric

detection method

-

detection method

-

shipped in

wet ice

shipped in

wet ice

shipped in

-

shipped in

dry ice

Application

Annexin V-FITC 凋亡检测试剂盒适于以下应用:
  • 在治疗前列腺癌的过程中对LNCaP前列腺癌细胞染色以测定 G. lucidum提取物活性。[1]
  • 在研究DBP-maf(维生素D结合蛋白-巨噬细胞活化因子)基因对前列腺癌细胞活性的抑制中,用于对肿瘤细胞的标记。[2]
  • 用于对flippase酶活性的间接测定。[3]

Features and Benefits

相比基于DNA的检测法(比如TUNEL法),可检测到细胞凋亡的更早期进程。
  • 快速标记细胞。细胞染色仅需10分钟。
  • 细胞无需固定或预处理,节省检测时间并满足细胞用于进一步研究。
  • 试剂盒内含碘化丙啶二级染料,用于从活细胞和坏死细胞中区分出凋亡细胞。

General description

Annexin V-FITC试剂盒可以荧光检测与annexin V结合的凋亡细胞,并使用流式细胞仪进行定量。AnnexinV-FITC试剂盒使用荧光素异硫氰酸酯(FITC)偶联的annexin V标记细胞膜表面的磷脂酰丝氨酸位点。该试剂盒包含碘化丙啶(PI),用于标记细胞膜完全破坏的坏死细胞内的DNA。这种组合可以区分早期凋亡细胞(annexin V阳性, PI阴性),坏死细胞(annexin V阳性, PI阳性),以及活细胞(annexin V阴性, PI阴性)。

Other Notes

使用前使所有组分达到室温。

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存储类别

10 - Combustible liquids


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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
Denise C Arruda et al.
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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
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
Ben-Zion Zaidman et al.
International journal of oncology, 31(4), 959-967 (2007-09-06)
Ganoderma lucidum (Curt.:Fr.) P. Karst, a medicinal fungus, has been widely used in Asian countries for centuries to prevent or treat a variety of diseases, including cancer. However, the mechanisms responsible for the effects of G. lucidum on cancer cells

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Questions

1–6 of 6 Questions  
  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 answer
    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.

      Helpful?

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

    1 answer
    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.

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

    1 answer
    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.

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

    1 answer
    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

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

    1 answer
    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.

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  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 answer
    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).

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