IL1RAPL2 Polyclonal Antibody (E-AB-90572)
For research use only.
| Verified Samples |
Verified Samples in WB: U-87MG |
| Dilution | WB 1:1000-1:2000 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | WB |
| Clonality | Polyclonal |
| Immunogen | Recombinant fusion protein of human IL1RAPL2 |
| Abbre | IL1RAPL2 |
| Synonyms | IL1R, IL-1R, TIGIRR, IL1RAPL2, IL-1R9, IL1R9, IL1RAPL-2, TIGIRR-1, IL 1 RAPL 2, IL 1 receptor accessory protein like 2, IL 1R 9, IL 1R9, IL 1RAPL 2, IL1 receptor accessory protein like 2, IL-1 receptor accessory protein-like 2, IL-1R-9, IL1RAPL 2, IL-1RAPL-2, IL-1-RAPL-2, IL1RAPL2 related protein, IL1RAPL-2-related protein, Interleukin 1 receptor 9, Interleukin 1 receptor accessory protein like 2, Interleukin-1 receptor 9, IRPL2_HUMAN, Three immunoglobulin domain containing IL1 receptor related 1, Three immunoglobulin domain-containing IL-1 receptor-related 1, TIGIRR 1, TIGIRR1, X linked interleukin 1 receptor accessory protein like 2, X-linked interleukin-1 receptor accessory protein-like 2 |
| Swissprot | |
| Calculated MW | 78 kDa |
| Observed MW |
80 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 | Membrane |
| Concentration | 1 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Neuroscience |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| background | The protein encoded by this gene is a member of the interleukin 1 receptor family. This protein is similar to the interleukin 1 accessory proteins, and is most closely related to interleukin 1 receptor accessory protein-like 1 (IL1RAPL1). This gene and IL1RAPL1 are located at a region on chromosome X that is associated with X-linked non-syndromic mental retardation. |
Other Clones
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Unconjugated
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