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Alexa Fluor® 647 Mouse anti-PKCα
Alexa Fluor® 647 Mouse anti-PKCα
Analysis of PKCa in lymphocytes.  [Left Panel] Human peripheral blood mononuclear cells (PBMC) were either stimulated with 10 μM Phorbol 12-myristate 13-acetate (PMA, Sigma-Aldrich, Cat. No. P8139) for 24 hours (shaded histogram) or unstimulated (open histogram).  The cells were fixed (BD Cytofix™ buffer, Cat. No. 554655) for 10 minutes, then permeabilized (BD Phosflow™ Perm Buffer III, Cat. No. 558050) on ice for at least 30 minutes, and then stained with Alexa Fluor® 647 Mouse anti-PKCα.  Lymphocytes were selected by scatter profile.  The data demonstrates that the expression of PKCα decreases when the lymphocytes are stimulated by PMA.  Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.  [Right Panel]  The specificity of mAb 3/PKCa was confirmed by western blot analysis using unconjugated antibody (Cat. No. 610107 or 610108) at 0.063 μg/ml on lysates from control (lane 1) and PMA-treated (lane 2) PBMC.  PKCa is identified as a band of 82 kDa, which decreases in intensity in the treated cells.  Purified Mouse anti-Actin monoclonal antibody (Cat. No. 612656 or 612657) was the gel-loading control.
Analysis of PKCa in lymphocytes.  [Left Panel] Human peripheral blood mononuclear cells (PBMC) were either stimulated with 10 μM Phorbol 12-myristate 13-acetate (PMA, Sigma-Aldrich, Cat. No. P8139) for 24 hours (shaded histogram) or unstimulated (open histogram).  The cells were fixed (BD Cytofix™ buffer, Cat. No. 554655) for 10 minutes, then permeabilized (BD Phosflow™ Perm Buffer III, Cat. No. 558050) on ice for at least 30 minutes, and then stained with Alexa Fluor® 647 Mouse anti-PKCα.  Lymphocytes were selected by scatter profile.  The data demonstrates that the expression of PKCα decreases when the lymphocytes are stimulated by PMA.  Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.  [Right Panel]  The specificity of mAb 3/PKCa was confirmed by western blot analysis using unconjugated antibody (Cat. No. 610107 or 610108) at 0.063 μg/ml on lysates from control (lane 1) and PMA-treated (lane 2) PBMC.  PKCa is identified as a band of 82 kDa, which decreases in intensity in the treated cells.  Purified Mouse anti-Actin monoclonal antibody (Cat. No. 612656 or 612657) was the gel-loading control.
製品詳細
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BD Phosflow™
Protein Kinase C α, PKC-α, PKC-A, PKCA, PRKCA
Human (QC Testing)
Mouse IgG2b, κ
Human PKCα aa. 270-427 Recombinant Protein
Intracellular staining (flow cytometry) (Routinely Tested)
20 µl
AB_1645435
Aqueous buffered solution containing BSA, protein stabilizer, and ≤0.09% sodium azide.
RUO


Preparation and Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to Alexa Fluor® 647 under optimum conditions, and unreacted Alexa Fluor® 647 was removed.

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Either BD Cytofix™ fixation buffer or BD Phosflow™ Fix Buffer I may be used for cell fixation.  Any of the three BD Phosflow™ permeabilization buffers may be used.

The purified format for this antibody has been reported to be reactive to human, mouse, rat, chicken, dog, and frog by western blotting (Cat. No. 610107 or 610108).

Product Notices

  1. This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-µl experimental sample (a test).
  2. Alexa Fluor® is a registered trademark of Molecular Probes, Inc., Eugene, OR.
  3. Alexa Fluor® 647 fluorochrome emission is collected at the same instrument settings as for allophycocyanin (APC).
  4. The Alexa Fluor®, Pacific Blue™, and Cascade Blue® dye antibody conjugates in this product are sold under license from Molecular Probes, Inc. for research use only, excluding use in combination with microarrays, or as analyte specific reagents. The Alexa Fluor® dyes (except for Alexa Fluor® 430), Pacific Blue™ dye, and Cascade Blue® dye are covered by pending and issued patents.
  5. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
  6. 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.
  7. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  8. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
560243 Rev. 2
抗体の詳細
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3/PKCα

The Protein Kinase C (PKC) family of homologous serine/threonine protein kinases is involved in a number of processes, such as growth, differentiation, and cytokine secretion.  At least eleven isozymes have been described.  These proteins are products of multiple genes and alternative splicing.  Conventional PKC (cPKC) subfamily members (α, β, and γ isoforms) consists of a single polypeptide chain containing four conserved regions (C) and five variable regions (V).  The N-terminal half containing C1, C2, V1, and V2 constitutes the regulatory domain and interacts with the PKC activators Ca2+, phospholipid, diacylglycerol, or phorbol ester.  However, the the C2-like domains of novel PKC (nPKC) subfamily members (δ, ε, η, and θ isoforms) are Ca2+-independent.  The atypical PKC (aPKC) subfamily members (ζ, ι, and λ isoforms) lack the C2 domain and are unique in that their activity is independent of diacylglycerols and phorbol esters. They also lack one repeat of the cysteine-rich sequences that are conserved in cPKC and nPKC members.  The C-terminal region of PKC contains the catalytic domain.  The PKC pathway represents a major signal transduction system that is activated following ligand-stimulation of transmembrane receptors by hormones, neurotransmitters, and growth factors.  PKCα regulates a wide variety of functions such as cellular growth, apoptosis, cardiomyocyte function, and brain cognitive functions.

The 3/PKCα monoclonal antibody recognizes PKCα, regardless of phosphorylation status, and has been reported to crossreact with PKCβ.

560243 Rev. 2
フォーマットの詳細
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Alexa Fluor™ 647
Alexa Fluor™ 647 Dye is part of the BD red family of dyes. This is a small organic fluorochrome with an excitation maximum (Ex Max) at 653-nm and an emission maximum (Em Max) at 669-nm. Alexa Fluor 647 is designed to be excited by the Red laser (627-640 nm) and detected using an optical filter centered near 520-nm (e.g., a 660/20 nm bandpass filter). Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
Alexa Fluor™ 647
Red 627-640 nm
653 nm
669 nm
560243 Rev.2
引用&参考文献
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Development References (6)

  1. Bivona TG, Quatela SE, Bodemann BO, et al. PKC regulates a farnesyl-electrostatic switch on K-Ras that promotes its association with Bcl-Xl on mitochondria and induces apoptosis . Mol Cell. 2006; 21(4):481-493. (Biology). View Reference
  2. Braz JC, Gregory K, Pathak A, et al. PKC-α regulates cardiac contractility and propensity toward heart failure. Nat Med. 2004; 10:248-254. (Biology). View Reference
  3. Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature. 1988; 334(6184):661-665. (Biology). View Reference
  4. Parker PJ, Murray-Rust J. PKC at a glance. J Cell Sci. 2004; 117:131-132. (Biology). View Reference
  5. Zhang XA, Bontrager AL, Hemler ME.. Transmembrane-4 superfamily proteins associate with activated protein kinase C (PKC) and link PKC to specific beta(1) integrins. J Biol Chem. 2001; 276(27):25005-25013. (Clone-specific: Immunofluorescence, Immunoprecipitation, Western blot). View Reference
  6. de Quervain D J-F, Papassotiropoulos A. Identification of a genetic cluster influencing memory performance and hippocampal activity in humans. Proc Natl Acad Sci U S A. 2006; 103(11):4270-4274. (Biology). View Reference
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560243 Rev. 2

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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.