Rabbit Recombinant Monoclonal PKC theta/PRKCQ antibody. Carrier free. Suitable for WB, ICC/IF, IHC-P and reacts with Mouse, Rat, Human samples.
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: PBS
Liquid
Monoclonal
WB | ICC/IF | IHC-P | |
---|---|---|---|
Human | Tested | Tested | Tested |
Mouse | Tested | Expected | Tested |
Rat | Tested | Expected | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Calcium-independent, phospholipid- and diacylglycerol (DAG)-dependent serine/threonine-protein kinase that mediates non-redundant functions in T-cell receptor (TCR) signaling, including T-cells activation, proliferation, differentiation and survival, by mediating activation of multiple transcription factors such as NF-kappa-B, JUN, NFATC1 and NFATC2. In TCR-CD3/CD28-co-stimulated T-cells, is required for the activation of NF-kappa-B and JUN, which in turn are essential for IL2 production, and participates in the calcium-dependent NFATC1 and NFATC2 transactivation. Mediates the activation of the canonical NF-kappa-B pathway (NFKB1) by direct phosphorylation of CARD11 on several serine residues, inducing CARD11 association with lipid rafts and recruitment of the BCL10-MALT1 complex, which then activates IKK complex, resulting in nuclear translocation and activation of NFKB1. May also play an indirect role in activation of the non-canonical NF-kappa-B (NFKB2) pathway. In the signaling pathway leading to JUN activation, acts by phosphorylating the mediator STK39/SPAK and may not act through MAP kinases signaling. Plays a critical role in TCR/CD28-induced NFATC1 and NFATC2 transactivation by participating in the regulation of reduced inositol 1,4,5-trisphosphate generation and intracellular calcium mobilization. After costimulation of T-cells through CD28 can phosphorylate CBLB and is required for the ubiquitination and subsequent degradation of CBLB, which is a prerequisite for the activation of TCR. During T-cells differentiation, plays an important role in the development of T-helper 2 (Th2) cells following immune and inflammatory responses, and, in the development of inflammatory autoimmune diseases, is necessary for the activation of IL17-producing Th17 cells. May play a minor role in Th1 response. Upon TCR stimulation, mediates T-cell protective survival signal by phosphorylating BAD, thus protecting T-cells from BAD-induced apoptosis, and by up-regulating BCL-X(L)/BCL2L1 levels through NF-kappa-B and JUN pathways. In platelets, regulates signal transduction downstream of the ITGA2B, CD36/GP4, F2R/PAR1 and F2RL3/PAR4 receptors, playing a positive role in 'outside-in' signaling and granule secretion signal transduction. May relay signals from the activated ITGA2B receptor by regulating the uncoupling of WASP and WIPF1, thereby permitting the regulation of actin filament nucleation and branching activity of the Arp2/3 complex. May mediate inhibitory effects of free fatty acids on insulin signaling by phosphorylating IRS1, which in turn blocks IRS1 tyrosine phosphorylation and downstream activation of the PI3K/AKT pathway. Phosphorylates MSN (moesin) in the presence of phosphatidylglycerol or phosphatidylinositol. Phosphorylates PDPK1 at 'Ser-504' and 'Ser-532' and negatively regulates its ability to phosphorylate PKB/AKT1. Phosphorylates CCDC88A/GIV and inhibits its guanine nucleotide exchange factor activity (PubMed:23509302).
PRKCD
Protein kinase C theta type, nPKC-theta, PRKCQ, PRKCT
Rabbit Recombinant Monoclonal PKC theta/PRKCQ antibody. Carrier free. Suitable for WB, ICC/IF, IHC-P and reacts with Mouse, Rat, Human samples.
Protein kinase C theta type, nPKC-theta, PRKCQ, PRKCT
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: PBS
Liquid
Monoclonal
Yes
EPR17074
Affinity purification Protein A
Blue Ice
+4°C
Do Not Freeze
ab250576 is the carrier-free version of Anti-PKC delta + PKC theta antibody [EPR17074] ab182127.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
This supplementary information is collated from multiple sources and compiled automatically.
PKC delta (Protein Kinase C delta) and PKC theta (Protein Kinase C theta) are members of the Protein Kinase C (PKC) family that function as serine/threonine kinases. These proteins with masses of approximately 78 kDa for PKC delta and 82 kDa for PKC theta play key roles in intracellular signaling processes. PKC delta is expressed in various tissues with particular abundance in heart lung and muscle. PKC theta is mainly found in T cells and skeletal muscle. Both proteins require calcium and diacylglycerol for activation and are often associated with lipid membranes where they exert their enzymatic activity.
PKC delta and PKC theta regulate diverse cellular processes including proliferation differentiation and apoptosis. PKC delta often participates in programmed cell death and is a part of several signaling cascades initiated by external stress signals. PKC theta is largely recognized for its function in immune response regulation particularly in T cell activation. These proteins are critical in forming signaling complexes with other molecules like scaffold proteins which helps in propagating their functional roles within the cell.
PKC delta and PKC theta are integral components of the MAPK (Mitogen-Activated Protein Kinase) and NF-kB (Nuclear Factor kappa-light-chain-enhancer of activated B cells) pathways. In the MAPK pathway PKC delta interacts significantly with proteins such as ERK and MEK mediating cell growth responses. PKC theta activates the NF-kB pathway in lymphocytes enhancing immune response and involving interaction with proteins like IkB kinase (IKK). These contributions show their impact on cellular events through precise regulation of signaling pathways.
PKC delta and PKC theta are linked to cancer and autoimmune diseases. PKC delta's regulation of apoptosis makes it a significant player in tumor suppression with alterations in its activity observed in several types of cancer. In autoimmune diseases such as rheumatoid arthritis PKC theta's role in T cell activity and cytokine production connects it to dysregulated immune responses. Both proteins interact with tumor suppressor p53 in cancer contexts revealing their importance in maintaining cellular equilibrium and responses to dysfunction.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
Active human PKC alpha full length protein (Recombinant human PKC alpha protein (Active) ab55672) contains aa1-672 with GST-tag; Active human PKC beta 1 full length protein (Recombinant human PKC beta 1 protein ab60840) contains aa1-671 with GST-tag; Active human PKC beta 2 full length protein (Recombinant human PKC beta 2 protein ab60841) contains aa1-673 with GST-tag; Active human PKC gamma full length protein (Recombinant human PKC gamma protein ab60842) contains aa1-677 with GST-tag; Active human PKC delta full length protein (Recombinant human PKC delta protein ab60844) contains aa1-676 with GST-tag; Active human PKC eta full length protein (Recombinant human PKC eta protein ab60849) contains aa1-683 with GST-tag; Active human PKC epsilon full length protein (Recombinant human PKC epsilon protein ab60847) contains aa1-737 with GST-tag; Active human PKC theta full length protein (Recombinant human PKC theta/PRKCQ protein ab56641) contains aa1-706 with GST-tag; Active human PKC mu full length protein (Recombinant human PKC mu/PKD protein ab60873) contains aa1-912 with GST-tag.
All lanes: Western blot - Anti-PKC delta + PKC theta antibody [EPR17074] (Anti-PKC delta + PKC theta antibody [EPR17074] ab182127) at 1/2000 dilution
Lane 1: Active human PKC alpha full length protein at 0.02 µg
Lane 2: Active human PKC beta 1 full length protein at 0.02 µg
Lane 3: Active human PKC beta 2 full length protein at 0.02 µg
Lane 4: Active human PKC gamma full length protein at 0.02 µg
Lane 5: Active human PKC delta full length protein at 0.02 µg
Lane 6: Active human PKC eta full length protein at 0.02 µg
Lane 7: Active human PKC epsilon full length protein at 0.02 µg
Lane 8: Active human PKC theta full length protein at 0.02 µg
Lane 9: Active human PKC mu full length protein at 0.02 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/50000 dilution
Predicted band size: 78 kDa, 82 kDa
Exposure time: 5s
5% NFDM/TBST: Blocking and diluting buffer.
Active human PKC alpha full length protein (Recombinant human PKC alpha protein (Active) ab55672) contains aa1-672 with GST-tag; Active human PKC beta 1 full length protein (Recombinant human PKC beta 1 protein ab60840) contains aa1-671 with GST-tag; Active human PKC beta 2 full length protein (Recombinant human PKC beta 2 protein ab60841) contains aa1-673 with GST-tag; Active human PKC gamma full length protein (Recombinant human PKC gamma protein ab60842) contains aa1-677 with GST-tag; Active human PKC delta full length protein (Recombinant human PKC delta protein ab60844) contains aa1-676 with GST-tag; Active human PKC eta full length protein (Recombinant human PKC eta protein ab60849) contains aa1-683 with GST-tag; Active human PKC epsilon full length protein (Recombinant human PKC epsilon protein ab60847) contains aa1-737 with GST-tag; Active human PKC theta full length protein (Recombinant human PKC theta/PRKCQ protein ab56641) contains aa1-706 with GST-tag; Active human PKC mu full length protein (Recombinant human PKC mu/PKD protein ab60873) contains aa1-912 with GST-tag.
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (Human epithelial cells from cervix adenocarcinoma) cells labeling PKC delta + PKC theta with Anti-PKC delta + PKC theta antibody [EPR17074] ab182127 at 1/200 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/400 dilution (green). Confocal image showing both cytoplasm and nuclear staining on HeLa cell line is observed. The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows:
1. Anti-PKC delta + PKC theta antibody [EPR17074] ab182127 at 1/200 dilution followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
2. Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/400 dilution.
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded human tonsil tissue labeling PKC delta + PKC theta with Anti-PKC delta + PKC theta antibody [EPR17074] ab182127 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on lymphocytes on germinal center of Human tonsil is observed. Counter stained with Hematoxylin.
Negative control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-PKC delta + PKC theta antibody [EPR17074] (Anti-PKC delta + PKC theta antibody [EPR17074] ab182127) at 1/2000 dilution
Lane 1: Mouse thymus lysates at 20 µg
Lane 2: Rat thymus lysates at 20 µg
Lane 3: Molt4 (Human lymphoblastic leukemia cell line) whole cell lysates at 20 µg
Lane 4: HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysates at 20 µg
All lanes: Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 78 kDa, 82 kDa
Observed band size: 78 kDa
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-PKC delta + PKC theta antibody [EPR17074] (Anti-PKC delta + PKC theta antibody [EPR17074] ab182127) at 1/2000 dilution
All lanes: Human fetal brain lysate at 10 µg
All lanes: Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 78 kDa, 82 kDa
Observed band size: 78 kDa
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-PKC delta + PKC theta antibody [EPR17074] (Anti-PKC delta + PKC theta antibody [EPR17074] ab182127) at 1/10000 dilution
Lane 1: Raw264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) whole cell lysates at 10 µg
Lane 2: Rat brain tissue lysate at 10 µg
Lane 3: Mouse brain tissue lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 103 kDa, 28 kDa, 39 kDa, 69 kDa, 78 kDa, 82 kDa
Observed band size: 104 kDa, 28 kDa, 40 kDa, 70 kDa, 78 kDa
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded human breast cancer tissue labeling PKC delta + PKC theta with Anti-PKC delta + PKC theta antibody [EPR17074] ab182127 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on cancer cells of Human breast carcinoma is observed. Counter stained with Hematoxylin.
Negative control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded mouse kidney cancer tissue labeling PKC delta + PKC theta with Anti-PKC delta + PKC theta antibody [EPR17074] ab182127 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary antibody at 1/500 dilution. Cytoplasmic staining on mouse kidney tubules is observed. Counter stained with Hematoxylin.
Negative control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
This data was developed using Anti-PKC delta + PKC theta antibody [EPR17074] ab182127, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded rat spleen cancer tissue labeling PKC delta + PKC theta with Anti-PKC delta + PKC theta antibody [EPR17074] ab182127 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on monocytes and macrophages on rat spleen is observed. Counter stained with Hematoxylin.
Negative control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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