Recombinant Rat FGFb Protein

Beta LifeScience SKU/CAT #: BL-1727NP
BL-1727NP: Greater than 95% as determined by reducing SDS-PAGE. (QC verified)
BL-1727NP: Greater than 95% as determined by reducing SDS-PAGE. (QC verified)

Recombinant Rat FGFb Protein

Beta LifeScience SKU/CAT #: BL-1727NP
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Product Overview

Description Recombinant Rat Fibroblast Growth Factor 2/Fibroblast Growth Factor Basic is produced by our E.coli expression system and the target gene encoding Ala11-Ser154 is expressed.
Accession P13109
Synonym Fibroblast Growth Factor 2; FGF-2; Basic Fibroblast Growth Factor; bFGF; Heparin-Binding Growth Factor 2; HBGF-2; FGF2; FGFB
Gene Background FGF-basic is a members of the Fibroblast Growth Factors (FGFs) family. The family constitutes a large family of proteins involved in many aspects of development including cell proliferation, growth, and differentiation. They act on several cell types to regulate diverse physiologic functions including angiogenesis, cell growth, pattern formation, embryonic development, metabolic regulation, cell migration, neurotrophic effects, and tissue repair. FGF-basic is a non-glycosylated heparin binding growth factor that is expressed in the brain, pituitary, kidney, retina, bone, testis, adrenal gland liver, monocytes, epithelial cells and endothelial cells. FGF-basic signals through FGFR 1b, 1c, 2c, 3c and 4.
Molecular Mass 16.2 KDa
Apmol Mass 16 KDa, reducing conditions
Formulation Lyophilized from a 0.2 μm filtered solution of 20mM PB, 150mM NaCl, pH 7.4.
Endotoxin Less than 0.1 ng/µg (1 EU/µg) as determined by LAL test.
Purity Greater than 95% as determined by reducing SDS-PAGE. (QC verified)
Biological Activity Biologically active. Please contact us to obtain bioactivity data.
Reconstitution Always centrifuge tubes before opening.Do not mix by vortex or pipetting.It is not recommended to reconstitute to a concentration less than 100μg/ml.Dissolve the lyophilized protein in distilled water.Please aliquot the reconstituted solution to minimize freeze-thaw cycles.
Storage Lyophilized protein should be stored at ≤ -20°C, stable for one year after receipt.Reconstituted protein solution can be stored at 2-8°C for 2-7 days.Aliquots of reconstituted samples are stable at ≤ -20°C for 3 months.
Shipping The product is shipped at ambient temperature.Upon receipt, store it immediately at the temperature listed below.
Usage For Research Use Only

Target Details

Target Function Acts as a ligand for FGFR1, FGFR2, FGFR3 and FGFR4. Also acts as an integrin ligand which is required for FGF2 signaling. Binds to integrin ITGAV:ITGB3. Plays an important role in the regulation of cell survival, cell division, cell differentiation and cell migration. Functions as a potent mitogen in vitro. Can induce angiogenesis. Mediates phosphorylation of ERK1/2 and thereby promotes retinal lens fiber differentiation.
Subcellular Location Secreted. Nucleus.
Protein Families Heparin-binding growth factors family
Database References
Tissue Specificity Found in all tissues examined.

Gene Functions References

  1. Dual delivery of bFGF and NGF binding coacervate was neuroprotective via stimulating the growth and proliferation of neurons. PMID: 29895019
  2. FGF2 protects against renal ischemia-reperfusion injury by attenuating mitochondrial damage and proinflammatory signaling. PMID: 28544332
  3. Study shows that fibroblast growth factor 2-ERK1/2 pathway is involved in the pathophysiology of depressive-like behaviors, and manipulating the neurogenesis pathway is a viable therapeutic approach to inflammation-associated depression. PMID: 28529071
  4. These findings may offer insight to help us understand more as to how bFGF ASODN can effectively suppress the proliferation and differentiation of NSCs. PMID: 28390174
  5. the present findings demonstrate that OCT alone or in combination with bFGF accelerates nerve repair in a large peripheral nerve defect in rats. PMID: 27529414
  6. Effect of basic fibroblast growth factor released from chitosan-fucoidan nanoparticles on neurite extension PMID: 23696519
  7. Thus, FGF2 is an alcohol-responsive gene constituting a positive regulatory feedback loop with alcohol. This loop leads to facilitation of alcohol consumption, marking FGF2 as a potential new therapeutic target for alcohol addiction. PMID: 28821667
  8. attempted to identify PKGII-targeted proteins, which are associated with the inhibition of FGF2-induced MAPK activation PMID: 28057484
  9. a moderate level of FGF-2 expression was observed in the cells within the connective tissue of the healing wounds of the normoglycemic group on all days evaluated which differed from that observed in the wounds of the diabetic group PMID: 27188585
  10. overexpression of BNIP3L in H9C2 cardiomyoblast cells reduced the cardioprotection of FGF-2 in hydrogen peroxide-induced necrosis and mitochondrial dysfunction. PMID: 28006775
  11. The induction of active beta-catenin and then fibronectin turnover in response to bFGF were markedly increased in pulmonary fibroblasts from rat with COPD. beta-Catenin/RhoA pathway results in ECM deposition in lung fibroblasts and myofibroblasts differentiation. PMID: 27734223
  12. It plays an important role as a key trigger of Intramuscular adipose tissue formation in vivo. PMID: 26154243
  13. This study demonstrated that altered Cx43 expression modulates bFGF expression, which correlates with prolactinoma development. PMID: 27078698
  14. Basic fibroblast growth factor increased in spinal microglia during the development of allodynia after spinal nerve ligation. PMID: 26583471
  15. TGF-beta1 was upregulated with FGF-2 treatment, and alpha-SMA expression induced by FGF-2 was inhibited after the cell was transferred with TGF-beta1 siRNA. PMID: 26729053
  16. Apocynin attenuated cardiac injury in type 4 radiorenal syndrome rats via inhibiting NADPH oxidase-dependent oxidative stress-activated ERK1/2 pathway and subsequent FGF-2 upregulation. PMID: 26109504
  17. Astrocyte-secreted FGF2 mediated stress-hormone-induced neural stem cell proliferation. PMID: 23599891
  18. Basic fibroblast growth factor and neurotrophin-3, which are released from astrocytes by exposure to thyroid hormone, influence each other to enhance Na+ current density in cultured hippocampal neurons. PMID: 26009773
  19. GK-2 had no effect on the expression level of FGFb and NT4, however, promoted an increase in the expression level of BDNF. PMID: 26571801
  20. FGF-2 in dissociated postnatal retinal cell cultures and found that FGF-2 is a potent factor triggering ganglion cell differentiation PMID: 25402196
  21. Regional differences in the FGF-2 expression pattern as either the first or the second injection of cocaine by themselves upregulated FGF-2 mRNA in the medial prefrontal cortex and nucleus accumbens while downregulating it in the hippocampus. PMID: 25124315
  22. fibroblast growth factor 2has roles in maintenance of the undifferentiated state and in proliferation of Endothelial progenitor cells , allowing EPC to maintain the potential to differentiate to Endothelial Cells. PMID: 24694617
  23. Subsarcolemmal mitochondria are more responsive than interfibrillar mitochondria to FGF-2-triggered protection from calcium-induced permeability transition, by a Cx43 channel-mediated pathway. PMID: 24654232
  24. It was found that cultivation of the cells under hypoxic conditions and bFGF is an optimum to maintain high viability and proliferation capacity of the mesenchymal stem cells. PMID: 25715620
  25. The learning impairment in IL-1beta-treated rats is accompanied by lower FGF-2 mRNA levels in medial prefrontal cortex and ventral (not dorsal) hippocampus, but TIMP-1 was not affected. PMID: 25697011
  26. astroglial cell maturation is enhanced by bFGF through induction of miR-134 PMID: 25482448
  27. bFGF-induced differentiation of dorsal root ganglia stem cells toward Schwann cells might be mediated by binding to fibroblast growth factor receptor-1 (FGFR-1) through activation of MAPK/ERK signal pathway. PMID: 24072480
  28. It is one of the key players in the origin and growth of neuronal and glial cells through autocrine and paracrine signaling. PMID: 24707873
  29. implicate FGF2 as a modifier of epigenetic mechanisms associated with emotional responsiveness, and point to H3K9me3 as a key player in the regulation of affective vulnerability PMID: 25071177
  30. enhanced protein kinase C levels, reduction of basic FGF expression, and increased in apoptosis might be associated with the development of diabetes-induced myoatrophy PMID: 24008114
  31. Studied the change of FGF-2 and IGF-1 in serum and bone callus after fracture in diabetic rats, and explored molecular biological mechanism of healing of diabetic fracture. PMID: 24418087
  32. TGF-beta1 and FGF2 induce the epithelial-mesenchymal transition of Hertwig's epithelial root sheath through a MAPK/ERK-dependent signaling pathway. PMID: 24610459
  33. Following FGF2 treatment, however, bHR-bLR differences in CCK and FGF-R1 mRNA expression were eliminated, due to decreased CCK mRNA levels PMID: 24121132
  34. Retinal injury may enhance neurotrophic factor expression in mesenchymal stem cells and promote the repair process. PMID: 24030359
  35. matrix proteoglycans such as perlecan serve as functional docking platforms for FGF2 in chronic transplant dysfunction. PMID: 24035513
  36. Basic fibroblast growth factor contributes to a shift in the angioregulatory activity of retinal glial (Muller) cells. PMID: 23861940
  37. With an increase in the degree of pressure ulcers, the expression of VEGF and bFGF in pressure ulcers tissue are decreased. This leads to a reduction in angiogenesis and may be a crucial factor in the formation of pressure ulcers. PMID: 23740668
  38. This study provides evidence that E and FGF2 exert a cooperative effect on the lactotroph proliferation principally by signaling initiated at the plasma membrane. PMID: 23651845
  39. Psychological stress could delay periodontitis healing in rats, which may be partly mediated by downregulation of the expression of bFGF in the periodontal ligament. PMID: 23326020
  40. We conclude that FGF-2 secreted by bone marrow-derived cells strongly increases early glial proliferation, which can potentially improve peripheral nervous system regeneration. PMID: 22793996
  41. FGF-2 induced the phosphorylation of Akt and its substrate, glycogen synthase kinase 3beta (GSK3beta) in addition to three MAP kinases in rat glioma cells. PMID: 22575563
  42. Spinal cord treatment of lesion with sciatic nerve and sciatic nerve plus FGF-2 allows recovery of hind limb movements compared to control, manifested by significantly higher behavioral scores after surgery. PMID: 22555431
  43. Inhibitng bFGF alleviates bleomycin-induced pulmonary fibrosis in rats. PMID: 20684286
  44. bFGF promote the proliferation and migration of endothelial progenitor cells, the effects of bFGF being implemented by activating ERK signalling through the expression of Pdgfrb. PMID: 22731705
  45. The epithelial and smooth muscle cell hyperplasia and increased Fgf-2 expression observed in this experimental model of obesity/insulin-resistance might explain the high frequency of benign prostatic hyperplasia in insulin-resistant men. PMID: 22661309
  46. bFGF gene expression is elevated following cerebral concussion, and might play an important role in cell degeneration and necrosis. PMID: 12857442
  47. Data suggest that molecular mechanism of dihydrotestosterone induction of Pfkfb4 (6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4) during spermatogenesis involves stimulation of Sertoli cells to secrete FGF-2. PMID: 22811469
  48. FGF-2 gene expression is significantly elevated from day 1 to day 14; the increase in FGF-2 protein level is most evident at day 7; cells expressing FGF-2 are primarily endothelial cells following myocardial infarction. PMID: 20674996
  49. The expression of VEGF and bFGF is significantly increased after stromal cell transplantation therapy during the late phase of acute myocardial infarction. PMID: 21162206
  50. astrocyte migration to injury sites may be a key factor in the repair mechanisms orchestrated by FGF2. PMID: 22189091

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Proteins are sensitive to heat, and freeze-drying can preserve the activity of the majority of proteins. It improves protein stability, extends storage time, and reduces shipping costs. However, freeze-drying can also lead to the loss of the active portion of the protein and cause aggregation and denaturation issues. Nonetheless, these adverse effects can be minimized by incorporating protective agents such as stabilizers, additives, and excipients, and by carefully controlling various lyophilization conditions.

Commonly used protectant include saccharides, polyols, polymers, surfactants, some proteins and amino acids etc. We usually add 8% (mass ratio by volume) of trehalose and mannitol as lyoprotectant. Trehalose can significantly prevent the alter of the protein secondary structure, the extension and aggregation of proteins during freeze-drying process; mannitol is also a universal applied protectant and fillers, which can reduce the aggregation of certain proteins after lyophilization.

Our protein products do not contain carrier protein or other additives (such as bovine serum albumin (BSA), human serum albumin (HSA) and sucrose, etc., and when lyophilized with the solution with the lowest salt content, they often cannot form A white grid structure, but a small amount of protein is deposited in the tube during the freeze-drying process, forming a thin or invisible transparent protein layer.

Reminder: Before opening the tube cap, we recommend that you quickly centrifuge for 20-30 seconds in a small centrifuge, so that the protein attached to the tube cap or the tube wall can be aggregated at the bottom of the tube. Our quality control procedures ensure that each tube contains the correct amount of protein, and although sometimes you can't see the protein powder, the amount of protein in the tube is still very precise.

To learn more about how to properly dissolve the lyophilized recombinant protein, please visit Lyophilization FAQs.

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