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
| Size | Price / USD | Stock | Quantity |
| 5MG | 133 | Get Quote |
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| 10MG | 206 | Get Quote |
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| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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Biological Information
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Product NameTAT 48-57
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NoteResearch use only, not for human use.
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Brief DescriptionTAT (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.
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DescriptionTAT (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.
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In VitroTAT (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.
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In Vivo——
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Synonyms——
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PathwayMicrobiology/Virology
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TargetHIV
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number253141-50-3
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Formula Weight1396.65
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Molecular FormulaC55H109N31O12
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (35.80 mM)
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SMILES——
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Chemical NameSequence:Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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