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Merck
CN

A2353

ATF-2 human

≥90% (SDS-PAGE), recombinant, expressed in E. coli, N-terminal maltose binding protein tagged, lyophilized powder

Synonym(s):

ATF-2 (AA 20-109)-Maltose Binding Protein fusion Protein, Activating transcription factor-2

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About This Item

UNSPSC Code:
12352202
NACRES:
NA.56
MDL number:
Form:
lyophilized powder
Assay:
≥90% (SDS-PAGE)
Biological source:
human
Recombinant:
expressed in E. coli
Mol wt:
53 kDa
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biological source

human

recombinant

expressed in E. coli

assay

≥90% (SDS-PAGE)

form

lyophilized powder

mol wt

53 kDa

technique(s)

activity assay: suitable

UniProt accession no.

storage temp.

−20°C

Quality Level

Gene Information

human ... ATF2(1386)

Physical form

Lyophilized powder in HEPES buffered salts containing NaCl, DTT, EGTA, Brij, trehalose, and protease inhibitors.

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

常规特殊物品
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T Herdegen et al.
Brain research. Brain research reviews, 28(3), 370-490 (1998-12-22)
This article reviews findings up to the end of 1997 about the inducible transcription factors (ITFs) c-Jun, JunB, JunD, c-Fos, FosB, Fra-1, Fra-2, Krox-20 (Egr-2) and Krox-24 (NGFI-A, Egr-1, Zif268); and the constitutive transcription factors (CTFs) CREB, CREM, ATF-2 and
C Livingstone et al.
The EMBO journal, 14(8), 1785-1797 (1995-04-18)
The ATF-2 transcription factor can mediate adenovirus E1A-inducible transcriptional activation. Deletion analysis has indicated that the N-terminal region of ATF-2 is essential for this response. Furthermore, the N-terminus can activate transcription in the absence of E1A when fused to a
Patrick J Metz et al.
Cell reports, 30(6), 1935-1950 (2020-02-13)
Alternative splicing is well understood to enhance proteome diversity as cells respond to stimuli. However, mechanistic understanding for how the spliceosome processes precursor messenger RNA (mRNA) transcripts to achieve template diversification is incomplete. We use recently developed enzymatic inhibitors of

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