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Purified Rabbit Anti-AIF w/control
(RUO)



Western blot analysis of AIF. Lysate from K-562 cells was probed with anti-AIF at dilutions of 1:1000 (lane 1), 1:2000 (lane 2), and 1:4000 (lane 3). AIF is identified as a band of ~67 kDa.


BD Pharmingen™ Purified Rabbit Anti-AIF w/control

Purified Rabbit Anti-AIF w/control
Regulatory Statusの凡例
Becton, Dickinson and Companyの書面による明示的な許諾を得た使用以外での製品の使用は固く禁じられています。
説明
Apoptosis is essential in maintaining normal cellular homeostasis and for normal development. Morphological as well as biochemical changes are a hallmark of apoptosis, and include membrane blebbing, chromosomal condensation and DNA fragmentation. The mitochondria plays an essential role in apoptosis. During apoptosis, the outer mitochondrial membrane (OMM) becomes permeable, releasing cytochrome c into the cytosol, which then binds Apaf-1 and in the presence of dATP/ATP can bind procaspase-9. Procaspase-9 is activated and forms a complex with cytochrome c/Apaf-1 called an apoptosome, which in turn can activate additional caspases, such as caspase-3. In addition to the release of cytochrome c, another protein has been identified, AIF (apoptosis-inducing factor), which is also released through the OMM. AIF has been cloned and has a predicted molecular weight of 57 kDa based upon its cDNA sequence. Characterization of AIF shows it to be a flavoprotein which has some homology to bacterial oxidoreductases. Upon induction of apoptosis, AIF translocates through the OMM to the cytosol and nucleus where it can initiate chromatin condensation. Bcl-2 can block the release of AIF from the mitochondria, but the apoptotic effect cannot be blocked if AIF has been released into the cytosol. Use of the pan caspase inhibitor, Z-VAD-FMK cannot block the phenotypic effects caused by AIF, indicating that AIF may act independently of caspases and Bcl-2 regulation. Furthermore, AIF has been shown to be essential for programmed cell death in murine embryonic morphogenesis and cavitation. Likewise, when AIF is genetically inactivated, embryonic stem cells are resistant to cell death following serum starvation. The antibodies recognize mouse, rat, and human AIF. A peptide corresponding to amino acids 517-531 of human AIF was used as the immunogen.
調製と保管
Store the antibody at 4°C, store positive control lysate (Cat. No. 51-16576N) at -20°C.
推奨アッセイ手順
Applications include western blot analysis (1:1000-1:4000). Store the antibody at 4°C. For long-term storage, the antibody may be stored at -20°C. Avoid multiple freeze-thaw cycles. K-562 control lysate [50 µg (1 µg/µl)] is provided as a positive control (Cat. No. 51-16576N; store lysate at -20°C). Additional K-562 control lysate (Cat. No. 611550) is sold separately as a ready-to-use western blot control. The antibodies are routinely tested by western blot analysis on K-562 cells.
製品通知
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
説明 | 数量/容量 | Part Number | EntrezGene ID |
---|---|---|---|
Purified Rabbit Anti-AIF | 100 µg (1 ea) | 51-8103KC | N/A |
K-562 Control Lysate | 50 µg (1 ea) | 51-16576N | N/A |
開発者向け参考資料 (3)
-
Joza N, Susin SA, Daugas E, et al. Essential role of the mitochondrial apoptosis-inducing factor in programmed cell death. Nature. 2001; 410(6828):549-554. (Biology). 参考文献を見る
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Martinou JC, Green DR. Breaking the mitochondrial barrier. Nat Rev Mol Cell Biol. 2001; 2(1):63-67. (Biology). 参考文献を見る
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Susin SA, Lorenzo HK, Zamzami N, et al. Molecular characterization of mitochondrial apoptosis-inducing factor. Nature. 1999; 397(6718):441-446. (Biology). 参考文献を見る
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
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