ABL1 Polyclonal Antibody

Verified Samples in IHC:Human breast caner

IHC 1:200-1:400

Polyclonal

IgG

Recombinant Human ABL1 protein expressed by E.coli

ABL1

ABL;bcr/abl;c-ABL;c-ABL1;JTK7;p150;v-abl

Cytoplasm > cytoskeleton. Nucleus. Sequestered into the cytoplasm through interaction with 14-3-3 proteins and Nucleus membrane. The myristoylated c-ABL protein is reported to be nuclear

Widely expressed

1mg/mL

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

PBS with 0.02% sodium azide,1% protective protein and 50% glycerol,pH7.4

Antigen Affinity Purification

Cancer;Epigenetics and Nuclear Signaling;Signal Transduction;Neuroscience;Metabolism;Cardiovascular;Biochemicals;Cell Biology;Developmental Biology;Immunology ;Stem Cells;Microbiology;Tags & Cell Markers;Isotype/Loading Controls

Unconjugated

c-Abl belongs to the class of tyrosine kinases and is the prototype of a subfamily which includes two members, c-Abl and Arg (Abl-related gene). Both proteins are localized at the cell membrane, actin cytoskeleton and cytosol, and c-Abl is present in the nucleus as well. c-Abl is a non-receptor tyrosine kinase that participates in multiple signaling pathways linking the cell surface, cytoskeleton, and the nucleus. Recent in vitro studies have also linked c-Abl to amyloid-beta-induced toxicity and tau phosphorylation. c-Abl has been implicated in many cellular processes including differentiation, division, adhesion, death, and stress response. c-Abl is a latent tyrosine kinase that becomes activated in response to numerous extra- and intra-cellular stimuli. The c-Abl protein is a ubiquitously expressed nonreceptor tyrosine kinase involved in the development and function of many mammalian organ systems, including the immune system and bone. It regulates the cellular response to TAM through functional interaction with the estrogen receptor, which suggests c-Abl as a therapeutic target and a prognostic tumor marker for breast cancer. c-Abl also plays a key role in signaling chemokine-induced T-cell migration. In addition, c-Abl contains NLSs (nuclear localization signals) and DNA-binding sequences important for nuclear functions. c-Abl has become an important therapeutic target in human chronic myeloid leukaemia.