C1QBP/HABP1 Monoclonal Antibody (AN200043P)
For research use only.
| Verified Samples | Verified Samples in WB: Hela, 293T, Jurkat, NIH/3T3 |
| Dilution | WB 1:500-1:2000, ICC/IF 1:20-1:100, IP 1-4 μL/mg of lysate |
| Isotype | IgG2b |
| Host | Mouse |
| Reactivity | Human |
| Applications | WB, ICC/IF, IP |
| Clonality | Monoclonal |
| Immunogen | Recombinant Human C1QBP / HABP1 protein |
| Abbre | C1QBP |
| Synonyms | HABP, SF2p, C1QBP, GC1QBP, HABP1, SF2p32, gC1Q-R, gC1qR, p32, ASF/SF2-Associated Protein p32, Complement Component 1 Q Subcomponent-Binding Protein Mitochondrial, gC1q-R Protein, Glycoprotein gC1qBP, Hyaluronan-Binding Protein 1, Mitochondrial Matrix Protein p32, p33 |
| Swissprot | |
| Calculated MW | 31 kDa |
| Observed MW |
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. |
| Concentration | 1 mg/mL |
| Buffer | 0.2 μm filtered solution in PBS |
| Purification Method | Protein A |
| Research Areas | Immunology, Microbiology |
| Clone No. | 11A9 |
| Conjugation | Unconjugated |
| Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
| Shipping | Ice bag |
| background | The human complement subcomponent C1q associates with C1r and C1s in order to yield the first component of the serum complement system. The protein encoded by this gene is known to bind to the globular heads of C1q molecules and inhibit C1 activation. This protein has also been identified as the p32 subunit of pre-mRNA splicing factor SF1, as well as a hyaluronic acid-binding protein. |
Other Clones
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Unconjugated
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