Recombinant Caspase-7 Monoclonal Antibody (AN301456L)
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For research use only.
| Verified Samples |
Verified Samples in WB: HeLa, RAW264.7, Jurkat Verified Samples in IHC: Human breast cancer, Human colon, Human liver cancer |
| Dilution | WB 1:500-1:2000, IHC 1:200-1:1000 |
| Isotype | IgG, κ |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | WB, IHC |
| Clonality | Monoclonal;Recombinant |
| Immunogen | Recombinant human Caspase-7 fragment |
| Abbre | Caspase-7 |
| Synonyms | MCH, LICE, Caspase-7 subunit p, ICE-like apoptotic protease, ICE-LAP, ICE LAP, CMH, CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3, caspase-7, Apoptotic protease MCH3, Apoptotic protease Mch-3, Caspase 7, Caspase 7 apoptosis related cysteine peptidase, Caspase7, Caspase-7 subunit p11, CMH 1, CMH1, ICE LAP3, ICE-like apoptotic protease 3 |
| Swissprot | |
| Calculated MW | 34 kDa |
| Observed MW |
18, 32, 35 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 | Cell Biology, Cancer, Metabolism |
| Clone No. | A151 |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | Ice bag |
| background | Involved in the activation cascade of caspases responsible for apoptosis execution. Cleaves and activates sterol regulatory element binding proteins (SREBPs). Proteolytically cleaves poly(ADP-ribose) polymerase (PARP) at a '216-Asp-|-Gly-217' bond. Overexpression promotes programmed cell death. |
Other Clones
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Unconjugated
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