Recombinant WWOX Monoclonal Antibody (AN301689L)
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For research use only.
| Verified Samples |
Verified Samples in WB: MCF-7, Mouse ovary, Rat brain Verified Samples in IHC: Human testis, Human cerebrum, Rat cerebrum Verified Samples in IF: MCF7, MDA-MB-231(Negative cell line) Verified Samples in FCM: MCF-7 |
| Dilution | WB 1:500-1:2000, IHC 1:50-1:100, IF 1:200-1:500, FCM 1:50 |
| Isotype | IgG, κ |
| Host | Rabbit |
| Reactivity | Human, Rat, Mouse |
| Applications | WB, IHC, IF, FCM |
| Clonality | Monoclonal;Recombinant |
| Immunogen | Recombinant human WWOX fragment |
| Abbre | WWOX |
| Synonyms | PRO, WOX, EIEE, SCAR, HHCMA, SDR41C, WWOX, D16S432E, EIEE28, FOR, FRA16D, HHCMA56, PRO0128, SCAR12, SDR41C1, WOX1, 5330426P09Rik, 9030416C10Rik, Aberrant WW domain-containing oxidoreductase, EC 1.1.1.-, Fragile site FRA16D oxidoreductase, Fragile site FRA16D Oxireductase, member 1, MGC55975, Putative oxidoreductase, Short chain dehydrogenase/reductase family 41C, WW domain containing oxidoreductase, WW domain-containing oxidoreductase, WW domain-containing protein WWOX, zgc:55975 |
| Swissprot | |
| Calculated MW | 47 kDa |
| Observed MW |
47 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, Nucleus |
| Concentration | 1 mg/mL |
| Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
| Purification Method | Protein A purified |
| Research Areas | Cell Biology, Neuroscience, Epigenetics and Nuclear Signaling, Cancer |
| Clone No. | A392 |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | Ice bag |
| background | Acts as a tumor suppressor and plays a role in apoptosis. May function synergistically with p53/TP53 to control genotoxic stress-induced cell death. Plays a role in TGFB1 signaling and TGFB1-mediated cell death. May also play a role in tumor necrosis factor (TNF)-mediated cell death. Inhibits Wnt signaling, probably by sequestering DVL2 in the cytoplasm. |
Other Clones
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