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TAT 48-57

CAS No. 253141-50-3

TAT 48-57( —— )

Catalog No. M30442 CAS No. 253141-50-3

TAT (48-57) is a cell-permeable peptide, derived from HIV-1 transactivator of transcription (Tat) protein residue 48-57.This peptide is amino acid residues 48 to 57 fragment of the basic domain of HIV Tat.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    TAT 48-57
  • Note
    Research use only, not for human use.
  • Brief Description
    TAT (48-57) is a cell-permeable peptide, derived from HIV-1 transactivator of transcription (Tat) protein residue 48-57.This peptide is amino acid residues 48 to 57 fragment of the basic domain of HIV Tat.
  • Description
    TAT (48-57) is a cell-permeable peptide, derived from HIV-1 transactivator of transcription (Tat) protein residue 48-57.This peptide is amino acid residues 48 to 57 fragment of the basic domain of HIV Tat.(In Vitro):TAT (48-57) is a cell-permeable peptide with short length, good at crossing cell membranes of different cell types, with overall low toxicity, and does not leak out from cells once internalised.
  • In Vitro
    TAT (48-57) is a cell-permeable peptide with short length, good at crossing cell membranes of different cell types, with overall low toxicity, and does not leak out from cells once internalised.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    HIV
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    253141-50-3
  • Formula Weight
    1396.65
  • Molecular Formula
    C55H109N31O12
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (35.80 mM)
  • SMILES
    ——
  • Chemical Name
    Sequence:Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

Cardozo AK, et al. Cell-permeable peptides induce dose- and length-dependent cytotoxic effects. Biochim Biophys Acta. 2007 Sep;1768(9):2222-34.
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