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M2435

c-Myc Peptide

≥97%, lyophilized powder

Synonym(e):

c-Myc tag

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Über diesen Artikel

UNSPSC Code:
12352202
NACRES:
NA.56
MDL number:

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Produktname

c-Myc Peptide, lyophilized powder

biological source

synthetic

assay

≥97%

form

lyophilized powder

mol wt

1203.3 Da

concentration

5-10 μg/mL (Suggested working concentration to compete out the binding of c-Myc)

technique(s)

protein extraction: suitable

storage temp.

−20°C

Quality Level

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Dieser Artikel
SAE0201SAB4200742SAB4301136
biological source

synthetic

biological source

-

biological source

mouse

biological source

rabbit

technique(s)

protein extraction: suitable

technique(s)

-

technique(s)

immunoblotting: 1:250-1:500 using lysate of HEK-293T cells over expressing c-Myc fusion protein, immunohistochemistry: suitable

technique(s)

western blot: 1:1000-1:5000 (Cell Lysate)

assay

≥97%

assay

-

assay

-

assay

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

100

form

lyophilized powder

form

suspension

form

lyophilized powder

form

buffered aqueous solution

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

General description

The c-Myc Peptide is a synthetic peptide with an amino acid sequence that corresponds to the amino acids 410-419 of the C-terminal of human c-myc.

Application

Useful for displacement of c-Myc-tagged fusion proteins bound to anti-c-Myc antibodies in immunoassays. The successful inhibition of antibody binding by c-Myc peptide demonstrates binding is specific.

Preparation Note

Dissolve in water to a final concentration of 5 mg/mL.

Other Notes

Amino acid sequence is corresponds to amino acids 410-419 of the C-terminal of human c-Myc.
Lyophilized from 0.1% TFA in H2O

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Atanas G Atanasov et al.
Biochimica et biophysica acta, 1783(8), 1536-1543 (2008-04-03)
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Survival of cancer cells in the harsh tumor microenvironment, characterized by oxygen and glucose deprivation, requires rapid initiation of cytoprotective measures. Metabolites whose levels change during stress are ideal signaling cues, particularly if used in post-translational modifications of stress-responsive signal

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