Anti-c-Myc Antibody (Monoclonal, 9E10)

$USD395

$USD19.75 Cashback

Description

Product Name: Anti-c-Myc Antibody (Monoclonal, 9E10)
Description Mouse IgG monoclonal antibody for c-Myc, v-myc myelocytomatosis viral
oncogene homolog (avian) (MYC) detection. Tested with WB, IHC-P, ICC in
Human. No cross reactivity with other proteins.
Host Mouse
Target Species Human
Application IHC-P, ICC, WB
Recommended Detection Systems
We recommend Enhanced Chemiluminescent Kit with anti-Mouse IgG(EK1001) for Western blot, and HRP Conjugated anti-Mouse IgG Super Vision Assay Kit (SV0001-1) for IHC(P) and ICC.
Immunogen Synthetic peptide corresponding to residues 408-439 of the human p62cMyc protein.
Specificity No cross reactivity with other proteins
Pack Size 100?g/vial
Catalog # Ab1028

Properties
Clonality Monoclonal
Clone Number 9E10
Form Lyophilized
Contents Mouse ascites fluid, 1.2% sodium acetate, 2mg BSA, with 0.01mg NaN3 as preservative.
*carrier free antibody available upon request

Reconstitution Add 1ml of PBS buffer will yield a concentration of 100ug/ml.
Storage At -20?C for one year. After reconstitution, at 4?C for one month. It can also be aliquoted and stored frozen at -20?C for a longer time. Avoid repeated freezing and thawing.
Purification Ascites

Background for Myc proto-oncogene protein:
C-Myc is an oncogene that functions both in the stimulation of cell proliferation and in apoptosis. c-Myc
elicits its oncogenic activity by causing immortalization, and to a lesser extent the transformation of cells,
in addition to several other mechanisms. The c-MYC proto-oncogene encodes a transcription factor that
is critical for cell growth and proliferation. It is one of the genes frequently altered in cancer cells in which
it exhibits constitutive activity. Downregulation of c-Myc is critical for 2-Methoxyestradiol(2ME2)-induced
oxidative stress and apoptosis in AML cells. And its up-regulation is important for promoting lymphocyte
cell division, and demonstrating that GFP-c-Myc expression is a marker of proliferating lymphocytes in
vivo.