Recombinant ABL1 Monoclonal Antibody (AN300847L)

For research use only.
Verified Samples | Verified Samples in WB: Hela |
Dilution | WB 1:2000-1:10000 |
Isotype | IgG,κ |
Host | Rabbit |
Reactivity | Human |
Applications | WB |
Clonality | Monoclonal;Recombinant |
Immunogen | Recombinant Human ABL1 protein |
Abbre | ABL1 |
Synonyms | JTK, Tyrosine-protein kinase ABL, Abelson tyrosine-protein kinase, Abelson murine leukemia viral oncogene homolog, ABL, JTK7, p150, c-ABL, v-abl, CHDSKM, c-ABL1, ABL1, bcr/abl, JTK7), Tyrosine-protein kinase ABL1, ABL1 (ABL), Abelson murine leukemia viral oncogene homolog 1, Abelson tyrosine-protein kinase 1, Abelson tyrosine protein kinase 1, Abl 1, ABL proto oncogene 1 non receptor tyrosine kinase, bcr/c abl oncogene protein, c ABL, c abl oncogene 1 non receptor tyrosine kinase, c abl oncogene 1 receptor tyrosine kinase, c ABL1, Proto oncogene tyrosine protein kinase ABL1, Proto-oncogene c-Abl, v abl, v abl Abelson murine leukemia viral oncogene homolog 1 |
Swissprot | |
Calculated MW | 123 kDa |
Observed MW |
123 kDa
Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include: 1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein. 2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes. 3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1. 4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids). 5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers. If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane. |
Cellular Localization | 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. |
Concentration | 0.2 mg/mL |
Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
Purification Method | Protein A |
Research Areas | Signal Transduction, Epigenetics and Nuclear Signaling, Cancer |
Clone No. | 5H6 |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | Ice bag |
background | This gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress. The activity of the protein is negatively regulated by its SH3 domain, whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA-binding activity that is regulated by CDC2-mediated phosphorylation, suggesting a cell cycle function. This gene has been found fused to a variety of translocation partner genes in various leukemias, most notably the t(9;22) translocation that results in a fusion with the 5' end of the breakpoint cluster region gene (BCR; MIM:151410). Alternative splicing of this gene results in two transcript variants, which contain alternative first exons that are spliced to the remaining common exons. |
Other Clones
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