Recombinant Neuropilin-1/NRP1/CD304 Monoclonal Antibody (AN300099P)
For research use only.
| Verified Samples |
Verified Samples in WB: Mouse heart in IF: MCF-7 |
| Dilution | WB: 1:1000；IHC-P: 1:100-1:500；ICC/IF: 1:100-1:200；FC: 1:50-1:100；IP: 1:20-1:50 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB, IHC-P, ICC/IF, FC, IP |
| Clonality | Recombinant;Monoclonal |
| Immunogen | Recombinant Human Neuropilin-1 / NRP1 / CD304 protein |
| Abbre | NRP1 |
| Synonyms | NPN, DKFZp686A, DKFZp781F, BDCA4, CD304, NP1, NRP, VEGF165R, Neuropilin-1, NRP1, ANG, NRP 1, NPN1, BDCA-4, DKFZp686A03134, DKFZp781F1414, Neuropilin1, CD304 antigen, neuropilin 1, Vascular endothelial cell growth factor 165 receptor, neuropilin-1, NRP1, NRPNP1 |
| Swissprot | |
| Calculated MW | 103 kDa |
| Observed MW |
120 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 | Secreted and Cell membrane. |
| Concentration | 1 mg/mL |
| Buffer | 0.2 μm filtered solution in PBS |
| Purification Method | Protein A |
| Research Areas | Cardiovascular, Neuroscience, Immunology |
| Clone | A1213 |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | Ice bag |
| background | This gene encodes one of two neuropilins, which contain specific protein domains which allow them to participate in several different types of signaling pathways that control cell migration. Neuropilins contain a large N-terminal extracellular domain, made up of complement-binding, coagulation factor V/VIII, and meprin domains. These proteins also contains a short membrane-spanning domain and a small cytoplasmic domain. Neuropilins bind many ligands and various types of co-receptors; they affect cell survival, migration, and attraction. Some of the ligands and co-receptors bound by neuropilins are vascular endothelial growth factor (VEGF) and semaphorin family members. Several alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2011] |
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