Anti-Human cMyc (Clone 9E10) - HRP

Referência C599-25

Tamanho : 25ug

Marca : Leinco Technologies

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AntiHuman cMyc [Clone 9E10] — HRP

Product No.: C599

Clone
9E10
Target
cMyc
Formats AvailableView All
Product Type
Hybridoma Monoclonal Antibody
Alternate Names
myc tag, cMyc tag, Myc epitope tag
Isotype
Mouse IgG1 κ
Applications
ELISA
,
FC
,
IF
,
IHC
,
IP
,
WB

Antibody Details

Product Details

Reactive Species
Epitope Tag
Host Species
Mouse
Immunogen
Cterminal region of human cmyc
Product Concentration
0.5 mg/ml
Formulation
This HRPconjugated antibody is formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 7.4, 1% BSA. (Warning: Use of sodium azide as a preservative will inhibit the enzyme activity of horseradish peroxidase)
State of Matter
Liquid
Storage and Handling
This horseradish peroxidase conjugated monoclonal antibody is stable when stored at 28°C. Do not freeze.
Regulatory Status
Research Use Only
Country of Origin
USA
Shipping
2 – 8° C Wet Ice
Additional Applications Reported In Literature ?
IHC,
IP,
IF,
WB,
ELISA,
FC
Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change.

Description

Description

Specificity
9E10 activity is directed against human cMyc and can crossreact with denatured murine cMyc in some circumstances.
Background
cMyc is an essential transcription factor that belongs to the superfamily of basic helixloop helix DNAbinding proteins that function in normal embryogenesis, acquisition and maintenance of stem cell properties, metabolism, cellular division, and cell death1, 2. cMyc is also a protooncogene, originally identified in Burkitt lymphoma1. Its dysregulation, by mutation or epigenetic modification, has been observed in over 50% of human cancers3. cMyc regulates various cancer cellular functions, including cell cycle, survival, proliferation, and metabolic reprogramming1, and is associated with tumor aggression and chemoresistance3. cMyc has been suggested as a target for cancer immunotherapy 2and various methods of inhibition have been studied1, 2, 3.

9E10 was generated by immunizing a BALB/c mouse with a synthetic peptide corresponding to residues 408432 of human cMyc conjugated to keyhole limpet hemocyanin via the cysteine residues4. Splenocytes were fused with SP2 myeloma cells. 9E10 failed to immunoprecipitate protein from Colo 320 HSR cell extracts during screening but did detect cMyc in Western blotting. The 9E10 epitope has become a wellknown affinity tag used in recombinant protein expression, i.e., the myctag5. The target epitope is the C terminal EQKLISEEDL peptide with the core sequence being LISE5and the crystal structure and binding mode have been solved6. 9E10 detection has highly variable epitope recognition that is dependent on neighboring sequence context7. Additionally, crossreactivity of 9E10 has been observed in murine cell lines in a fluorescence assay and by Western blotting8.

Antigen Distribution
cMyc is ubiquitously expressed during tissue development and in a wide variety of tumors. cMyc is often studied in embryonic stem cells and induced pluripotent stem cells. cMyc is mainly associated with cell nuclei.
NCBI Gene Bank ID
UniProt.org
Research Area
Cell Biology
.
Epitope Tag

References & Citations

1 Yoshida GJ. J Exp Clin Cancer Res. Jul 27;37(1):173. 2018.
2 Llombart V, Mansour MR. EBioMedicine. 75:103756. 2022.
3 Fatma H, Maurya SK, Siddique HR. Semin Cancer Biol. 83:166176. 2022.
4 Evan GI, Lewis GK, Ramsay G, et al. Mol Cell Biol. 5(12):36103616. 1985.
5 Hilpert K, Hansen G, Wessner H, et al. Protein Eng. 14(10):803806. 2001.
6 Krauss N, Wessner H, Welfle K, et al. Proteins. 73(3):552565. 2008.
7 Schüchner S, Behm C, Mudrak I, et al. Sci Signal. 28;13(616):eaax9730. 2020.
8 Siegel J, Brandner G, Hess RD. Int J Oncol. 13(6):12591262. 1998.
9 Varughese M, Chi A, Teixeira AV, et al. Mol Med. 4(2):8795. 1998.
10 Fan H, Villegas C, Chan AK, et al. Biochem Cell Biol. 76(1):125128. 1998.
11 Chan S, Gabra H, Hill F, et al. Mol Cell Probes. 1(1):7382. 1987.
12 Porter MJ, Field JK, Leung SF, et al. Acta Otolaryngol. 114(1):105109. 1994.
13 O'Leary JJ, Landers RJ, Crowley M, et al. J Clin Pathol. 50(11):896903. 1997.
14 Feller K, Yang S, Tung N, et al. J Eur Acad Dermatol Venereol. 28(1):120124. 2014.
15 Baker AM, Van Noorden S, RodriguezJusto M, et al. Histopathology. 69(2):222229. 2016.