Ugrás a tartalomra
Merck

ROAMYC

Roche

Anti-c-myc

from mouse IgG1κ

Szinonimák:

anti-myc

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
12352203
klón:
9E10, monoclonal
application:
DB
ICC
IHC
IP
WB
technika/technikák:
dot blot: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
citations:
16

biológiai forrás

mouse

Minőségi szint

konjugátum

unconjugated

antitest forma

purified immunoglobulin

antitest terméktípus

primary antibodies

klón

9E10, monoclonal

Teszt

90% (SDS-PAGE)

Forma

frozen liquid (11667203001)
lyophilized (11667149001)

kiszerelés

pkg of 200 μg (11667149001)
pkg of 5 mg (11667203001 [1 ml])

gyártó/kereskedő neve

Roche

technika/technikák

dot blot: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

izotípus

IgG1κ

epitóp szekvencia

EQKLISEEDL

tárolási hőmérséklet

−20°C

Általános leírás

Anti-c-myc is a monoclonal antibody to c-myc peptide (clone 9E10). Anti-c-myc recognizes the 9E10 epitope sequence (EQKLISEEDL), derived from the human c-myc protein. The monoclonal antibody against the c-myc epitope is well characterized and does not cross-react with other cellular proteins. The antibody recognizes its antigenic determinant even when the c-myc peptide epitope is introduced into unrelated recombinant proteins by a technique known as epitope tagging.
The cellular myelocytomatosis (c-myc) is the cellular homologue of the v-myc gene originally isolated from an avian myelocytomatosis virus. The gene encoding it is mapped to human chromosome 8q24. It c-myc is a member of MYC gene family. c-Myc gene codes for basic helix-loop-helix/leucine zipper (bHLH/LZ) transcription factor that regulates the G1-S cell cycle transition.


Contents:
  • 11 667 149 001: lyophilizate, stabilized
  • 11 667 203 001: frozen solution, (5 mg/ml)

Egyediség

Anti-c-myc recognizes the amino acid sequence EQKLISEEDL, which was derived from the human c-myc protein. The antibody recognizes its antigenic determinant even when the c-myc peptide epitope is introduced into unrelated recombinant proteins either N-terminal, C-terminal or internal. The monoclonal antibody against the c-myc epitope is well characterized and does not crossreact with other cellular proteins.

Immunogén

Amino acid sequence EQKLISEEDL was derived from the human c-myc protein.

Alkalmazás

Use Anti-c-myc for the detection of native human c-myc protein and recombinant epitope-tagged proteins that contain the c-myc epitope using:
  • Dot blots
  • Immunocytochemistry
  • Immunoprecipitation
  • Western blots
  • Immunohistochemistry.

Biokémiai/fiziológiai hatások

The cellular myelocytomatosis (c-myc) oncogene has a crucial role in cellular proliferation, differentiation, apoptosis and acts as transcriptional regulator of gene expression. c-myc expression is essential and sufficient to assist most of the cells to enter DNA synthetic (S) phase of the cell cycle. The encoded protein plays a crucial role in vasculogenesis and angiogenesis during cancer development and progression. c-myc interacts with its binding partner Max and activates the transcription of growth promoting genes such as cyclin D2 and ornithine decarboxylase. It also represses the transcription of multiple genes, especially p21 and p27, by binding to the transcription initiator element (Inr) in a complex with Max and either Sp1 (specificity protein 1) or Miz1 (Myc-interacting zinc finger protein 1). Overexpression of MYC in DLBCL (diffuse large B-cell lymphoma) results in poor outcome and invasive treatment when medicated with rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP).

Minőség

Anti-c-myc antibody is tested for functionality and purity relative to a reference standard to confirm the quality of each new reagent lot.

Elkészítési megjegyzés

Working concentration: Working concentration of conjugate depends on application and substrate.

The following concentrations should be taken as a guideline:
  • Western blot: 1 to 10 μg/ml


Working solution: Tris-buffered saline containing 0.1% Tween 20.

Feloldás

Add 500 μl PBS to a final concentration of 400 μg/ml.

Analízis megjegyzés

The monoclonal antibody against the c-myc epitope is well characterized and does not crossreact with other cellular proteins. No cross reaction with murine c-myc.

Egyéb megjegyzések

For life science research only. Not for use in diagnostic procedures.

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Tárolási osztály kódja

11 - Combustible Solids

Lobbanási pont (F)

does not flash

Lobbanási pont (C)

does not flash


Válasszon a legfrissebb verziók közül:

Analitikai tanúsítványok (COA)

Lot/Batch Number

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Ha egy adott verzióra van szüksége, a tétel- vagy cikkszám alapján rákereshet egy adott tanúsítványra.

Már rendelkezik ezzel a termékkel?

Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.

Dokumentumtár megtekintése

Ines B Folger et al.
Nature chemical biology, 20(6), 761-769 (2024-02-03)
Engineered biosynthetic assembly lines could revolutionize the sustainable production of bioactive natural product analogs. Although yeast display is a proven, powerful tool for altering the substrate specificity of gatekeeper adenylation domains in nonribosomal peptide synthetases (NRPSs), comparable strategies for other
Apoptotic signaling by c-MYC.
Hoffman B and Liebermann D A
Oncogene, 27(50), 6462-6472 (2008)
HIF-2alpha promotes hypoxic cell proliferation by enhancing c-myc transcriptional activity.
Gordan JD, et al.
Cancer Cell, 11(4), 335-347 (2007)
R Dalla-Favera et al.
Proceedings of the National Academy of Sciences of the United States of America, 79(24), 7824-7827 (1982-12-01)
Human sequences related to the transforming gene (v-myc) of avian myelocytomatosis virus (MC29) are represented by at least one gene and several related sequences that may represent pseudogenes. By using a DNA probe that is specific for the complete gene
Over-expression of the c-myc proto-oncogene in colorectal carcinoma.
Smith DR, et al.
British Journal of Cancer (1993)

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