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          目錄:上海貝博生物科技有限公司>>Primary Antibodies>> ADAMTS-2 rabbit pAb

          ADAMTS-2 rabbit pAb
          • ADAMTS-2 rabbit pAb
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          SourceRabbitApplicationsWB,ELISAReactivityHumanDilutionWB:1:500-1:2000
          • Source

            Rabbit

          • Applications

            WB,ELISA

          • Reactivity

            Human

          • Dilution

            WB: 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.

          • Storage

            -20°C/1 year

          • Specificity

            ADAMTS-2 Polyclonal Antibody detects endogenous levels of ADAMTS-2 protein.

          • Source/Purification

            The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

          • Immunogen

            Synthesized peptide derived from ADAMTS-2 . at AA range: 1140-1220

          • Uniprot No

            O95450

          • Alternative names

            ADAMTS2; PCINP; PCPNI; A disintegrin and metalloproteinase with thrombospondin motifs 2; ADAM-TS 2; ADAM-TS2; ADAMTS-2; Procollagen I N-proteinase; PC I-NP; Procollagen I/II amino propeptide-processing enzyme; Procollagen N-endopeptidase; pNPI

          • Form

            Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

          • Clonality

            Polyclonal

          • Isotype

            IgG

          • Background

            ADAM metallopeptidase with thrombospondin type 1 motif 2(ADAMTS2) Homo sapiens This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically

          • Other

            ADAMTS2, A disintegrin and metalloproteinase with thrombospondin motifs 2

          • Mol.Wt (Da)

            134723

          • Concentration

            1 mg/ml

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