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Purified Mouse Anti-Jun
Purified Mouse Anti-Jun
Western blot analysis of c-Jun. Lane 1, recombinant c-Jun. Lane 2, BSA (negative control). Lane 3, Cos-7 cell lysate (negative control). Lane 4, Cos-7 lysate from cells which were transiently transfected with c-Jun. Anti-Jun identifies both recombinant c-Jun protein (lane 1) as well as c-Jun which is expressed in Cos-7 cells (lane 4) as an ~39 kDa band.
Western blot analysis of c-Jun. Lane 1, recombinant c-Jun. Lane 2, BSA (negative control). Lane 3, Cos-7 cell lysate (negative control). Lane 4, Cos-7 lysate from cells which were transiently transfected with c-Jun. Anti-Jun identifies both recombinant c-Jun protein (lane 1) as well as c-Jun which is expressed in Cos-7 cells (lane 4) as an ~39 kDa band.
Product Details
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BD Pharmingen™
Human (QC Testing)
Mouse IgG1
Recombinant C-terminal half of c-Jun
Western blot (Routinely Tested), Gel shift (Tested During Development)
39 kDa, (c-Jun), 35 kDa (JunB), 40-50 kDa (JunD)
0.5 mg/ml
AB_395230
Aqueous buffered solution containing ≤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 4°C.

Recommended Assay Procedures

We recommend to use 1-2 µg/ml of antibody concentration for western blot application.

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.
554083 Rev. 8
Antibody Details
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G56-206

The cellular Jun (c-Jun) and its viral counterpart, v-Jun, are efficient  transcriptional activators.  Both c-Jun and v-Jun are sequence-specific DNA-binding proteins that recognize the same sequence motif, termed TRE (TPA responsive element). c-Jun does not recognize this motif unless it forms a heteromeric complex with c-fos, forming the transcription factor AP1. Jun family members JunB and JunD are 44% and 45% identical to c-Jun on the protein level, respectively. Jun family members are highly conserved between species. There is 98% amino acid identity between human and mouse c-Jun, and 45% between chicken and mouse c-Jun. There is 98% amino acid homology between human and mouse JunB, 95% between human and rat JunB, and 99.5% between mouse and rat JunB. There is 77% amino acid homology between human and mouse JunD and 71% between chicken and mouse JunD.

G56-206 recognizes Jun family members including c-Jun, JunB, and JunD. A truncated recombinant protein consisting of the C-terminal half of c-Jun was used as immunogen. This region contains the c-Jun DNA binding domain. The antibody was evaluated by western blot analysis using in vitro translated c-Jun and Cos-7 monkey kidney cells transfected with recombinant c-Jun.

554083 Rev. 8
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
554083 Rev.8
Citations & References
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Development References (3)

  1. Angel P, Karin M. The role of Jun, Fos and the AP-1 complex in cell-proliferation and transformation. Biochim Biophys Acta. 1991; 1072(2-3):129-157. (Biology). View Reference
  2. Curran T, Bravo R, Müller R. Transient induction of c-fos and c-myc in an immediate consequence of growth factor stimulation. Cancer Surv. 1987; 4(4):655-681. (Biology). View Reference
  3. In: Hesketh R. The Oncogene Handbook. New York: Academic Press; 1994:236-252.
554083 Rev. 8

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.