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Merck

SRP0253

4EBP1 Active human

recombinant, expressed in E. coli, ≥70% (SDS-PAGE)

Sinonimo/i:

EIF4EBP1, Eukaryotic translation initiation factor 4E binding protein 1, PHAS-I, Phosphorylated heat- and acid-stable protein regulated by insulin 1, eIF4E-binding protein 1

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100 μG

CHF 572.00

CHF 572.00


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Informazioni su questo articolo

UNSPSC Code:
12352202
NACRES:
NA.32
MDL number:

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Nome del prodotto

4EBP1 Active human, recombinant, expressed in E. coli, ≥70% (SDS-PAGE)

biological source

human

recombinant

expressed in E. coli

assay

≥70% (SDS-PAGE)

form

aqueous solution

mol wt

13.6 kDa

packaging

pkg of 100 μg

storage condition

avoid repeated freeze/thaw cycles

concentration

>0.02 mg/mL

NCBI accession no.

UniProt accession no.

shipped in

dry ice

storage temp.

−70°C

Gene Information

human ... EIF4EBP1(1978)

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SRP5161SRP5162WH0001978M1
Gene Information

human ... EIF4EBP1(1978)

Gene Information

human ... EIF4EBP1(1978)

Gene Information

human ... EIF4EBP1(1978)

Gene Information

human ... EIF4EBP1(1978)

biological source

human

biological source

human

biological source

human

biological source

mouse

assay

≥70% (SDS-PAGE)

assay

≥70% (SDS-PAGE)

assay

≥70% (SDS-PAGE)

assay

-

form

aqueous solution

form

buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

form

buffered aqueous solution

recombinant

expressed in E. coli

recombinant

expressed in E. coli

recombinant

expressed in baculovirus infected Sf9 cells

recombinant

-

concentration

>0.02 mg/mL

concentration

-

concentration

-

concentration

-

Application

4EBP1 Active human has been used as a substrate for in vitro kinase assay.[1]

Biochem/physiol Actions

E1F4EBP1 (eukaryotic translation initiation factor 4E binding protein 1) is involved in protein synthesis, cell growth and survival. In unphosphorylated form, it suppresses the translation initiation of capped mRNAs. On the other hand, in phosphorylated form, it increases translation initiation.[2] Phosphorylation of E1F4EBP1 releases it from eIF4E (eukaryotic translation initiation factor 4E), thereby resulting in cap-dependent translation.[3] E1F4EBP1 is also involved in tumorigenesis and the gene is overexpressed in various carcinomas.[2][3] It is also a substrate for mTORC1 (mammalian target of rapamycin complex 1). In non-phosphorylated conditions, it interacts with p21 (cyclin-dependent kinase inhibitor) and enhances destabilization of p21.[4]

General description

The gene E1F4EBP1 (eukaryotic translation initiation factor 4E binding protein 1) is mapped to human chromosome 8p11-p12.[5] It belongs to the translation repressor protein family.[3]
Human E1F4EBP1 (eukaryotic translation initiation factor 4E binding protein 1)(GenBank Accession No. NM_004095), full length with N-terminal His tag, MW = 13.6kDa, expressed in Escherichia coli.

Physical form

Formulated in 50 mM Tris-HCl, pH 7.5, 150 mM NaCl, 0.25 mM DTT, 0.1 mM EGTA, 0.1 mM EDTA, 0.1 mM PMSF and 50% glycerol.

Preparation Note

Thaw on ice. Upon first thaw, briefly spin tube containing enzyme to recover full content of the tube. Aliquot enzyme into single use aliquots. Store remaining undiluted enzyme in aliquots at -70°C. Note: Enzyme is very sensitive to freeze/thaw cycles.

Classe di stoccaggio

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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MicroRNAs 125a and 125b inhibit ovarian cancer cells through post-transcriptional inactivation of EIF4EBP1.
Lee M, et al.
Oncotarget, 7, 8726-8726 (2016)
p53 Deletion or Hotspot Mutations Enhance mTORC1 Activity by Altering Lysosomal Dynamics of TSC2 and Rheb.
Agarwal S, et al.
Molecular Cancer Research, 14, 66-66 (2016)
Multiple interacting oncogenes on the 8p11-p12 amplicon in human breast cancer.
Yang ZQ, et al.
Cancer Research, 66, 11632-11632 (2006)
Chao Zhang et al.
PloS one, 4(3), e4881-e4881 (2009-03-19)
Deregulation of the phosphatidylinositol 3-kinases (PI3K)/Akt/mammalian target of rapamycin (mTOR) pathway plays a central role in tumor formation and progression, providing validated targets for cancer therapy. S9, a hybrid of alpha-methylene-gamma-lactone and 2-phenyl indole compound, possessed potent activity against this
Naoto Tatewaki et al.
PloS one, 11(1), e0147570-e0147570 (2016-01-30)
Ataxia telangiectasia mutated (ATM) kinase plays a crucial role as a master controller in the cellular DNA damage response. Inhibition of ATM leads to inhibition of the checkpoint signaling pathway. Hence, addition of checkpoint inhibitors to anticancer therapies may be

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