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      產(chǎn)品中心

      Recombinant Human TGF-beta 1
      EPT005
      規(guī)格: 價(jià)格:
      10μg ¥1800.00

      Overview

      Product name: Recombinant Human TGF-beta 1
      Description: Recombinant Human Transforming Growth Factor Beta 1 is produced by our Mammalian expression system and the target gene encoding Ala279-Ser390 is expressed.
      Accession: P01137
      Molecular weight: 12.8 KDa
      Apparent molecular weight: 13 KDa, reducing conditions
      Purity: Greater than 95% as determined by reducing SDS-PAGE.
      Endotoxin: Less than 0.01 EU/μg as determined by LAL test.
      Biological activity: Measured by its ability to inhibit the IL-4-dependent proliferation of TF?1 human erythroleukemic cells. The ED50 for this effect is 4-40 pg/ml.
      Redissolve: Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles.?
      Storage: Lyophilized protein should be stored at < -20°C, though stable at room temperature for 3 weeks. Reconstituted protein solution can be stored at 4-7°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
      Delivery condition: The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature listed below.
      Background: Transforming Growth Factor β-1 (TGFβ-1) is a secreted protein which belongs to the TGF-β family. TGFβ-1 is abundantly expressed in bone, articular cartilage and chondrocytes and is increased in osteoarthritis (OA). TGFβ-1 performs many cellular functions, including the control of cell growth, cell proliferation, cell differentiation and apoptosis. The precursor is cleaved into a latency-associated peptide (LAP) and a mature TGFβ-1 peptide. TGFβ-1 may also form heterodimers with other TGFβ family members. It has been found that TGFβ-1 is frequently upregulated in tumor cells. Mutations in this gene results in Camurati-Engelmann disease.
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