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Key Documents

T1331

Sigma-Aldrich

Tat-Beclin 1

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About This Item

Linear Formula:
Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Gly-Gly-Thr-Asn-Val-Phe-Asn-Ala-Thr-Phe-Glu-Ile-Trp-His-Asp-Gly-Glu-Phe-Gly-Thr
CAS Number:
Molecular Weight:
3741.10
UNSPSC Code:
12352200
NACRES:
NA.32

Assay

≥95% (HPLC)

Quality Level

form

lyophilized powder

shipped in

dry ice

storage temp.

−20°C

General description

The TAT-BECLIN-1 (autophagy activator) peptide is derived from a region of the autophagy protein, beclin 1, attached to the HIV-1 Tat protein transduction domain. The peptide includes 11 amino acids at the N terminus derived from the Tat protein transduction domain, 18 amino acids (267–284 aa) from beclin 1 at the C terminus and a GG linker.

Biochem/physiol Actions

The TAT-BECLIN-1 (autophagy activator) peptide reduces the accumulation of polyglutamine aggregates and pathogen replication in vitro. This peptide is also found to reduce the mortality of mice infected by different viruses. The TAT-BECLIN-1 peptide is predicted to stimulate cell death via autophagy.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Autosis is a Na+, K+-ATPase?regulated form of cell death triggered by autophagy-inducing peptides, starvation, and hypoxia?ischemia.
Liu Y, et al.
Proceedings of the National Academy of Sciences of the USA, 110(51), 20364-20371 (2013)
Identification of a candidate therapeutic autophagy-inducing peptide.
Shoji-Kawata S, et al.
Nature, 494(7436), 201-201 (2013)
Sangam Rajak et al.
Molecular metabolism, 53, 101286-101286 (2021-07-06)
Crinophagy is a secretory granule-specific autophagic process that regulates hormone content and secretion in endocrine cells. However, despite being one of the earliest described autophagic processes, its mechanism of action and regulation in mammalian cells remains unclear. Here, we examined

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