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  • bsm-33189M增強型青色熒光蛋白單克隆抗體

    Cyan Fluorescent Protein (CFP) is a genetic mutant of green fluorescent protein (GFP) originally derived from the jellyfish Aequorea victoria. The fluorescence of EYFP was detected with an excitation filter of 485 nm and an emission filter of 545 nm, and that of ECFP was detected with filters of 420 and 486 nm (Perkin Elmer), respectively. In the present reporter assay, EYFP and ECFP were selected as a reporter protein and an internal control for normalization of transfection, respectively

    更新時間:2025-02-26
    型號:bsm-33189M
    廠商性質:生產廠家
    瀏覽量:127
  • bsm-33183M亮橙色熒光蛋白單克隆抗體

    更新時間:2025-02-26
    型號:bsm-33183M
    廠商性質:生產廠家
    瀏覽量:133
  • bs-20157RHSV tag標簽抗體

    HSV tag is a peptide epitope tag, sequence: QPELAPEDPED.

    更新時間:2025-02-26
    型號:bs-20157R
    廠商性質:生產廠家
    瀏覽量:160
  • bsm-33215MNano-Tag (9)單克隆抗體

    Well-characterized antibodies for epitope tags consisting of short sequences are widely used in the study of protein expression in various systems. The Nano-tag is a new streptavidin-binding peptide for both the purification and the detection of Nano-tagged proteins. This peptide possesses nanomolar-affinity for streptavidin and therefore is termed Nano-tag. The nano-tags have two types, Nano-tag15 (MDVEAWLGARVPLVET) and Nano-tag9 (MDVEAWLGAR), which bind to streptavidin with dissociation co

    更新時間:2025-02-26
    型號:bsm-33215M
    廠商性質:生產廠家
    瀏覽量:165
  • bs-33017RS-tag標簽抗體

    S-tag is the name of an oligopeptide derived from pancreatic ribonuclease A (RNase A). If RNase A is digested with subtilisin, a single peptide bond is cleaved, but the resulting two products remain weakly bound to each other and the protein, called ribonuclease S, remains active although each of the two products alone shows no enzymatic activity. The N-terminus of the original RNase A, also called S-peptide, consists of 20 amino acid residues, of which only the first 15 are required for ribon

    更新時間:2025-02-26
    型號:bs-33017R
    廠商性質:生產廠家
    瀏覽量:156
  • bsm-33133MTAP-Tag(標簽)單克隆抗體

    Tandem affinity purification (TAP) is a purification technique for studying protein–protein interactions. It involves creating a fusion protein with a designed piece, the TAP tag, on the end. The original TAP method involves the fusion of the TAP tag to the C-terminus of the protein under study. The TAP tag consists of calmodulin binding peptide (CBP) from the N-terminal, followed by tobacco etch virus protease (TEV protease) cleavage site and Protein A, which binds tightly to IgG. The relati

    更新時間:2025-02-26
    型號:bsm-33133M
    廠商性質:生產廠家
    瀏覽量:136
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