WB: Use at a concentration of 1 - 10 μg/ml. Detects a band of approximately 30 kDa (predicted molecular weight: 31 kDa). Optimal dilutions/concentrations should be determined by the end user.
HeLa Cell Lysate, Mouse Brain Tissue Extract, Rat Brain Tissue Extract
This antibody detects an ~30 kDa protein, corresponding to the apparent molecular mass of 14-3-3 beta, 14-3-3 epsilon or 14-3-3 zeta on SDS-PAGE immunoblots, in samples from human, mouse and rat origins.
Preservative: None Constituents: 50% Glycerol, PBS. pH 7.2
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
1 mg/ml (Please refer to the vial label for the specific concentration.)
Human 14-3-3 beta fusion protein.
Protein A purified
For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
1433 beta + epsilon + zeta, 1433, GW128, 14-3-3E, 14-3-3-zeta, HS1, FLJ45465, KCIP-1, FLJ53559, MGC111427, YWHAA, MGC126532, MDCR, MGC138156, MDS, YWHAD, KCIP 1, 14 3 3 zeta, KCIP1, 1433zeta
14-3-3 proteins are highly conserved proteins which play a role in both signal transduction and progression through the cell cycle by binding to and regulating several different proteins. 14-3-3 proteins activate tyrosine and tryptophan hydroxylases and protein kinase C. They mediate signal transduction by binding to phosphoserine-containing proteins. There are at least 7 mammalian isoforms: alpha, beta, gamma, delta, epsilon, zeta, and eta. An eighth subtype, termed theta has been found in rat brain. The 14-3-3 proteins exists in vitro and in vivo as either homo- or heterodimers which interact via their N-terminal domains and are subject to phosphorylation by protein kinase C. 14-3-3 proteins are localized in the cytoplasm of neurons in the cerebral cortex and are axonally transported to the nerve terminals. They may be present at lower levels in various other eukaryotic tissues. Northern blot analysis has shown expression of the eta chain in cultured cell lines derived from various tumors.