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Purified Mouse Anti-PKCθ (pT538)
Purified Mouse Anti-PKCθ (pT538)
Jurkat cells were treated with Anti-CD3 and were then either left untreated (lane 1) or treated (lane 2) with 200 U/ml of lambda phosphatase for 1 hr at 37°C. The top panel was probed with anti-PKCθ (Cat. No. 610089) and the bottom panel was probed with anti-PKCθ (pT538).
Jurkat cells were treated with Anti-CD3 and were then either left untreated (lane 1) or treated (lane 2) with 200 U/ml of lambda phosphatase for 1 hr at 37°C. The top panel was probed with anti-PKCθ (Cat. No. 610089) and the bottom panel was probed with anti-PKCθ (pT538).
Product Details
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BD Transduction Laboratories™
Human (QC Testing)
Mouse IgG2a
Phosphorylated Human PKCθ Peptide
Western blot (Routinely Tested), Immunohistochemistry-formalin (antigen retrieval required) (Tested During Development)
79 kDa
250 µg/ml
AB_399954
Aqueous buffered solution containing BSA, glycerol, and ≤0.09% sodium azide.
RUO


Preparation And Storage

The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. Store undiluted at -20°C.

Product Notices

  1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  2. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  3. 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.
  4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
612735 Rev. 1
Antibody Details
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19/PKC

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. Three categories exist, conventional PKC (cPKC), novel PKC (nPKC), and atypical PKC (aPKC). These proteins are products of multiple genes and alternative splicing and have different modes of activation. For example, cPKC's members (α, βI, βII, and γ)  are calcium activated, phospholipid-dependent serine/threonine specific enzymes which can also be activated by phorbol esters. However, the novel PKC (nPKC) subfamily members (δ , ε, η, and θ isoforms) and the atypical PKC (PKC) subfamily members (ζ , í , and λ isoforms) are Ca[2+] independent. The aPKC members are unique in that their activity is independent of diacylglycerols and phorbol esters. The PKC pathway represents a major signal transduction system that is activated following ligand-stimulation of transmembrane receptors by hormones, neurotransmitters and growth factors. PKCθ transcripts are expressed in most tissues with the highest levels being found in hematopoietic tissues and cell lines, including T cells and thymocytes. PKCθ RNA is readily detectable in skeletal muscle, lung, and brain. However, PKCθ expression is not detected in several human carcinoma cell lines. Abundant  expression of this PKC isozyme in hematopoietic cells suggests that it may have a role in growth and differentiation processes of these cells.

The 9/PKC monoclonal antibody recognizes the phosphorylated threonine 538 (pT538) of human PKCθ.

612735 Rev. 1
Format Details
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Purified
Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
Purified
612735 Rev.1
Citations & References
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View product citations for antibody "612735" on CiteAb

Development References (2)

  1. Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature. 1988; 334(6184):661-665. (Biology). View Reference
  2. Soderling TR. Protein kinases. Regulation by autoinhibitory domains. J Biol Chem. 1990; 265(4):1823-1826. (Biology). View Reference
612735 Rev. 1

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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.