Recombinant FASN Monoclonal Antibody (AN301520L)
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For research use only.
| Verified Samples |
Verified Samples in WB: HeLa, 293T, A549, HepG2, MOLT-4, PC-3 Verified Samples in IHC: Human liver, Human lung adenocarcinoma, Mouse liver, Rat liver Verified Samples in FCM: A549 Verified Samples in IP: HeLa cells extracts |
| Dilution | WB 1:500-1:2000, IHC 1:200-1:1000, FCM 1:50-1:100, IP 1:25-1:50 |
| Isotype | IgG, κ |
| Host | Rabbit |
| Reactivity | Human, Rat, Mouse |
| Applications | WB, IHC, FCM, IP |
| Clonality | Monoclonal;Recombinant |
| Immunogen | Recombinant human FASN fragment |
| Abbre | FASN |
| Synonyms | SDR27X, FASN, FAS, OA-519, SDR27X1, fatty acid synthase, Type I fatty acid synthase, IAPP, FAS, fatty acid synthase, OA-519, SDR27X1 |
| Swissprot | |
| Calculated MW | 273 kDa |
| Observed MW |
260 kDa
The actual band is not consistent with the expectation.
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 |
| Concentration | 1 mg/mL |
| Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
| Purification Method | Protein A purified |
| Research Areas | Cardiovascular, Signal Transduction, Neuroscience, Cancer, Metabolism |
| Clone No. | A219 |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | Ice bag |
| background | Fatty acid synthetase is a multifunctional enzyme that catalyzes the de novo biosynthesis of long-chain saturated fatty acids starting from acetyl-CoA and malonyl-CoA in the presence of NADPH. This multifunctional protein contains 7 catalytic activities and a site for the binding of the prosthetic group 4'-phosphopantetheine of the acyl carrier protein ([ACP]) domain. |
Other Clones
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Unconjugated
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