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      Purified Mouse Anti-SC35
      Purified Mouse Anti-SC35
      Western blot analysis of SC35. Lysates from MG-63 human osteosarcoma cells were probed with anti-SC35 (clone αSC35, Cat. No. 556363). SC35 is detected as a band of ~35 kDa.
      Purified Mouse Anti-SC35
      Western blot analysis of SC35. Lysates from MG-63 human osteosarcoma cells were probed with anti-SC35 (clone αSC35, Cat. No. 556363). SC35 is detected as a band of ~35 kDa.
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      BD Pharmingen™
      Human (QC Testing)
      Mouse IgG1, κ
      Partially purified spliceosomes
      Western blot (Routinely Tested), Immunofluorescence (Tested During Development), Immunoprecipitation (Reported)
      0.5 mg/ml
      AB_396388
      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.
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      Recommended Assay Procedures

      Staining is nuclear, a punctate or speckled nuclear pattern may be detected. Only a subset of cells are stained, the percentage may vary between cell type and experimental conditions. MG-63 human osteosarcoma, HeLa carcinoma (ATCC CCL-2), or BRL-3A rat liver cells (ATCC CRL-1442) are suggested as positive controls.

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      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.
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      556363 Rev. 6
      Antibody Details
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      αSC35

      SC35 belongs to a highly conserved SR splicing factor family. Members of this family have characteristic RNA-binding domains and serine/arginine-rich (SR) motifs. SR proteins are expressed in the nucleus and are essential pre-messenger RNA splicing factors. Nuclear pre-messenger RNA takes place in spliceosomes, multicomponent complexes consisting of five small nuclear ribonucleoprotein particles (U1, U2, U4, U5, U6) and other non-snRNP factors such as SC35. SC35 is necessary for an early step in spliceosome assembly and can also influence the selection of alternative splice sites. SC35 is identified as a 35 kDa protein in SDS/PAGE.

      Clone αSC35 has been shown to recognize SC35 in human, and rat cells. However, it should recognize SC35 from any species, as SC35 is conserved from Drosophila to man. Partially purified spliceosomes were used as immunogen.

      556363 Rev. 6
      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
      556363 Rev.6
      Citations & References
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      View product citations for antibody "556363" on CiteAb

      Development References (3)

      1. Fu XD, Maniatis T. Factor required for mammalian spliceosome assembly is localized to discrete regions in the nucleus. Nature. 1990; 343(6257):437-441. (Immunogen: Immunofluorescence, Western blot). View Reference
      2. Fu XD. Specific commitment of different pre-mRNAs to splicing by single SR proteins. Nature. 1993; 365(6441):82-85. (Biology). View Reference
      3. Sukegawa J, Blobel G. A putative mammalian RNA helicase with an arginine-serine-rich domain colocalizes with a splicing factor. J Biol Chem. 1995; 270(26):15702-15706. (Clone-specific: Immunofluorescence). View Reference
      556363 Rev. 6

      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.