Recombinant bFGF/FGF2 Monoclonal Antibody (AN300097P)
For research use only.
| Verified Samples | Verified Samples in WB:HeLa |
| Dilution | WB: 1:1000;ICC/IF: 1:200-1:500;FC: 1:200-1:500;IP: 1:20-1:50 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | WB, ICC/IF, FC, IP |
| Clonality | Recombinant;Monoclonal |
| Immunogen | A synthetic peptide corresponding to the N-terminus of the Human bFGF. |
| Abbre | FGF2 |
| Synonyms | HBGF, FGF, BFGF, FGF-2, FGFB, HBGF-2, Basic FGF, FGF2, Basic Fibroblast Growth Factor, B-FGF, FGF-β, Fibroblast Growth Factor 2, heparin-binding growth factor 2, prostatropin, BFGF, B-FGF, FGF-2, FGFB, fibroblast growth factor 2, HBGF-2, heparin-binding growth factor 2, prostatropin, basic, Basic fibroblast growth factor bFGF, FGF 2, FGF B, FGF2 basic, Fibroblast growth factor, Fibroblast growth factor 2 (basic), HBGF 2, HBGF2, HBGH 2, HBGH2, Heparin binding growth factor 2 precursor, heparin-binding growth factor 2, FGF-β |
| Swissprot | |
| Calculated MW | 31 kDa |
| Observed MW |
19 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, Nucleus. |
| Tissue Specificity | Expressed in granulosa and cumulus cells. Expressed in hepatocellular carcinoma cells, but not in non-cancerous liver tissue. |
| Concentration | 1 mg/mL |
| Buffer | 0.2 μm filtered solution in PBS |
| Purification Method | Protein A |
| Research Areas | Cardiovascular, Signal Transduction, Neuroscience, Stem Cells, Cancer, Developmental Biology |
| Clone | A1211 |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | Ice bag |
| background | The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members bind heparin and possess broad mitogenic and angiogenic activities. This protein has been implicated in diverse biological processes, such as limb and nervous system development, wound healing, and tumor growth. The mRNA for this gene contains multiple polyadenylation sites, and is alternatively translated from non-AUG (CUG) and AUG initiation codons, resulting in five different isoforms with distinct properties. The CUG-initiated isoforms are localized in the nucleus and are responsible for the intracrine effect, whereas, the AUG-initiated form is mostly cytosolic and is responsible for the paracrine and autocrine effects of this FGF. [provided by RefSeq, Jul 2008] |
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