Recombinant Mouse Interferon beta (Ifnb1)

Code CSB-YP011048MO
MSDS
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Source Yeast
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Code CSB-EP011048MO
MSDS
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Source E.coli
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Code CSB-EP011048MO-B
MSDS
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Source E.coli
Conjugate Avi-tag Biotinylated
E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.
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Code CSB-BP011048MO
MSDS
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Source Baculovirus
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Code CSB-MP011048MO
MSDS
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Source Mammalian cell
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Product Details

Purity
>85% (SDS-PAGE)
Target Names
Ifnb1
Uniprot No.
Alternative Names
Ifnb1; Ifb; IfnbInterferon beta; IFN-beta
Species
Mus musculus (Mouse)
Expression Region
22-182
Target Protein Sequence
INYKQLQLQ ERTNIRKCQE LLEQLNGKIN LTYRADFKIP MEMTEKMQKS YTAFAIQEML QNVFLVFRNN FSSTGWNETI VVRLLDELHQ QTVFLKTVLE EKQEERLTWE MSSTALHLKS YYWRVQRYLK LMKYNSYAWM VVRAEIFRNF LIIRRLTRNF QN
Protein Length
Full Length of Mature Protein
Tag Info
Tag type will be determined during the manufacturing process.
The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
Form
Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
Buffer before Lyophilization
Tris/PBS-based buffer, 6% Trehalose, pH 8.0
Reconstitution
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
Troubleshooting and FAQs
Storage Condition
Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
Shelf Life
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
Lead Time
Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
Notes
Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
Datasheet
Please contact us to get it.

Customer Reviews and Q&A

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Target Background

Function
Has antiviral, antibacterial and anticancer activities.
Gene References into Functions
  1. IFNbeta activates neuronal PI3K/Akt signalling and Akt binds to transcription factor FoxA1 that translocates to the nucleus and induces PDL1. Conversely, inhibition of PI3K/Akt, FoxA1 and PDL1 blocked neuronal ability to generate FoxA1(+)Tregs. PMID: 28436428
  2. Macrophages activated by metabolic endotoxemia infiltrated into islets and produced IFNbeta, which induced beta-cell apoptosis by increasing the expression of Xaf1. PMID: 29132171
  3. Reactive oxygen species (ROS) scavenger N-acetyl cysteine (NAC) prevented mitochondrial dysfunctions, type I IFN-stimulated transcript levels, inflammatory cell infiltrate, and muscle weakness in an experimental autoimmune myositis mouse model. Thus, these data highlight a central role of mitochondria and ROS in dermatomyositis . PMID: 28623559
  4. Nontypeable Haemophilus influenzae DNA as a Pathogen-Associated Molecular Pattern Molecules triggered I-IFN response, which was STING/TBK1/IRF3 dependent. PMID: 29421524
  5. The Lipopolysaccharide and IFN-beta-mediated increase of STAT1 mRNA and protein levels was abrogated by chelation of Zn(2+) with the membrane permeable chelator N,N,N',N'-Tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) in RAW 264.7 macrophages. PMID: 28965604
  6. MAVS is essential for spontaneous high basal expression of IFN-beta in cardiac myocytes and the heart. PMID: 28822807
  7. Mycobacterium smegmatis induces higher Ifnb expression in macrophages than Mycobacterium avium subspecies. PMID: 28422568
  8. Chronic presence of IFN-I in the brain microenvironment, which negatively affects cognitive function, is mediated via modulation of microglial activity. PMID: 28959042
  9. In experimental autoimmune encephalomyelitis, IFN-beta inhibited downstream inflammatory cytokines through the inhibition of PI3K/AKT/NF-kappaB axis and p38, JNK-MAPK, as well as the regulation of mTOR complexes. Moreover, IFN-beta inhibited Th17 differentiation and influenced the acetylation of the Il17a and Opn gene promoters. IFN-beta plays a role in Th17 differentiation partly through the inhibition of OPN. PMID: 29127843
  10. This review briefly discusses the dysregulation of main T cell subpopulations in CNS autoimmunity and summarized the T cell targeted effects of endogenous and exogenous IFN-beta in health and EAE/MS, with emphasis on the direct actions of IFN-beta on each T cell subset involved in the disease. PMID: 27033173
  11. Rb selectively inhibits innate IFN-beta production by enhancing deacetylation of Ifnb1 promoter, exhibiting a previous unknown non-classical role in innate immunity, which also suggests a role of Rb in the regulation of type I IFN production in inflammatory or autoimmune diseases. PMID: 27267461
  12. The effect of topical TREX1 knockdown and local interferon production on HIV transmission in human cervicovaginal explants and humanized mice, is reported. PMID: 27184854
  13. The TBK1 Y179A mutant failed to rescue type I IFN production by virally infected RAW264.7 macrophages deficient in TBK1. PMID: 28049762
  14. The data demonstrate that an atypical TLR7 signaling pathway contributes to type interferon-beta expression during Y. pestis infection and suggest that the TLR7-driven type I IFN response plays an important role in determining the outcome of plague. PMID: 28847850
  15. Long-term exposure to atmospheric particulates, PM2.5 up-regulated H3K4 and H3K9 methylation in IL-6 and IFN-beta promoter regions through down-regulating Kdm6a expression. The results suggest that short-term exposure to PM2.5 significantly enhances the survival rate of influenza A-contaminated mice, while long-term PM2.5 inhalation lowers the capacity of pulmonary macrophages to secrete IL-6 and IFN-beta. PMID: 28887033
  16. Extracellular ATP reduces the replication of VSV, Newcastle disease virus, murine leukemia virus and HSV in vivo and in vitro through the P2X7 receptor; ATP increases IFN-beta expression. Mechanistically, ATP facilitates IFN-beta secretion through P38/JNK/ATF-2 signaling pathways, which are crucial in promoting antiviral immunity. PMID: 28687662
  17. study reports that mitochondrial antiviral signaling protein (MAVS), -mediated IFN-alpha/beta production and IFNAR signaling are required for alloimmune responses to the human K1 Ag in a murine model of inflammation-induced alloimmunization PMID: 28630094
  18. study identifies a novel role for RIPK1 and RIPK3, a pair of homologous serine/threonine kinases previously implicated in the regulation of necroptosis and pathologic tissue injury, in directing IFN-beta production in macrophages PMID: 28461567
  19. results suggest that, in addition to its well-known signaling activity, IFN-beta may be directly antimicrobial and be part of a growing family of cytokines and chemokines, called kinocidins, that also have antimicrobial properties. PMID: 28411186
  20. results show that resistance to HSV-1 in the trigeminal ganglia during acute infection is conferred in part by STING and IFN-alpha/beta signaling in both bone marrow-derived and -resident cells, which coalesce to support a robust HSV-1-specific CD8(+) T cell response PMID: 27511736
  21. RIPK3 regulates type I IFN both transcriptionally, by interacting with MAVS and limiting RIPK1 interaction with MAVS, and post-transcriptionally. PMID: 28410401
  22. neddylation contributes to HSV-1-induced early phase IFN-beta production. PMID: 27593482
  23. Rubicon specifically interacts with the interferon regulatory factor (IRF) association domain (IAD) of IRF3, and this interaction leads to inhibition of the dimerization of IRF3, which negatively regulates interferon-mediated antiviral response. PMID: 28468885
  24. Translation arrest is further demonstrated to be key for anti-viral response by acting synergistically with MAVS activation to amplify TBK1 signaling and IFN-beta mRNA transcription, while GADD34-dependent protein synthesis recovery contributes to the heterogeneous expression of interferon observed in dsRNA-activated cells. PMID: 28100675
  25. The authors report that Raf kinase inhibitory protein (RKIP) is essential for TBK1 activation and type I interferon production triggered by viral infection. PMID: 27753621
  26. this study shows that paracrine type I IFN can profoundly enhance innate recognition and TLR2-dependent transcriptional responses to Francisella tularensis infection upstream of its role in inflammasome regulation in primary murine peritoneal macrophages but not murine bone marrow-derived macrophages PMID: 27231145
  27. STAT2 recruits USP18 to the type I IFN receptor subunit IFNAR2 via its constitutive membrane-distal STAT2-binding site. PMID: 28165510
  28. In the exorbital lachrymal gland, the mRNA expression of IFN beta and IFN alpha (type I IFNs) was weak- to strong-positive at 1 days post inoculation (DPI), and became negative at 2DPI. PMID: 27079771
  29. TBK1 complexes required for the phosphorylation of IRF3 and the production of interferon-beta have been identified. PMID: 28159912
  30. The authors conclude that IFN-alphabeta is pathogenic during chronic Mycobacterium africanum infection and that the pathogenic effects may be mediated through poorer control of bacterial growth. PMID: 27803172
  31. IRF-1 and interferon-alpha with interferon-beta cooperate to control acute gammaherpesvirus infection. PMID: 27795415
  32. this study shows that endosomal signalling by Lactobacillus acidophilus that leads to IFN-beta production is inhibited by TLR stimulation from the plasma membrane PMID: 27441725
  33. Truncated rabies virus phosphoprotein isoforms promote viral replication in muscle cells through their IFN-beta antagonist activities and thereby support infection of peripheral nerves. PMID: 27384657
  34. identify iNOS/NO as an integral component of IFN-beta production in response to dsRNA in hepatocytes in a pathway that involves the coordinated activities of TLR3/Trif and PKR PMID: 27226571
  35. Data show that using adipose-derived mesenchymal stem cells (AD-MSCs) expressing interferon-beta (IFN-beta) as an anti-inflammatory agent, offer evidence supporting that the stem cell therapies in experimental autoimmune encephalomyelitis (EAE) may improve the valuable effects of IFN-beta in the autoimmune disease. PMID: 27373971
  36. NLRX1 was observed to reduce interferon beta and cytokines in response to HIV-1 reverse-transcribed DNA. PMID: 27078069
  37. This study establishes IL-1beta and IFN-I levels as key homeostatic variables of protective, yet tuned, immune responses against severe invasive bacterial infection. PMID: 26962946
  38. Type I IFN Does Not Promote Susceptibility to Foodborne Listeria monocytogenes PMID: 26895837
  39. Results suggest that the lack of autocrine response to interferon-betaI by the host cell may be one mechanism for maintenance of respiratory syncytial virus persistence. PMID: 26501312
  40. TRIM33 deficiency results in high expression of Ifnb1 at late stages of macrophages activation. PMID: 26592194
  41. Inhibition of PI3K or Akt abrogated the ability of Syk deficiency to enhance IFNbeta and IL-10 in Syk deficient cells PMID: 26708990
  42. IFN-beta significantly attenuated the progression of liver fibrosis, with accompanying transcriptional downregulation of the TLR4 adaptor molecule MyD88. PMID: 25715168
  43. Thus, despite their use of the same receptor, IFNbeta and IFNalpha have unique and distinguishable biologic functions, with IFNbeta being mainly responsible for promoting lymphocytic choriomeningitis virus persistence. PMID: 25974304
  44. Mice lacking Ifnb function exhibited motor and cognitive learning impairments with accompanying alpha-synuclein-containing Lewy bodies in the brain, as well as a reduction in dopaminergic neurons and defective dopamine signaling in the nigrostriatal region. PMID: 26451483
  45. Data show that interferon beta knockout IFN-beta(-/-) mice exhibit greater resistance to Salmonella typhimurium infection. PMID: 26202980
  46. results indicate that Lyn plays a positive regulatory role in RIG-I-mediated interferon expression as a downstream component of IPS-1 PMID: 25585356
  47. Data show that decreased type I interferon gene expression in T cell subsets of human CASP8 and FADD-like apoptosis regulating protein c-FLIPS transgenic female mice. PMID: 24816846
  48. Data suggest that Brd4 (bromodomain containing 4) is essential for Toll-like receptor-stimulated interferon-beta (Ifnb) gene transcription by permitting transcription factors to interact with the Ifnb promoter in macrophages. PMID: 25891802
  49. PP1 directly interacts with IRF3 and dephosphorylates IRF3 at Ser385 and Ser396, resulting in the suppression of TLR- and RLR-triggered IFN-beta production. PMID: 25239187
  50. Interferons alpha and beta control propagation of long interspersed element-1. PMID: 25716322

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Subcellular Location
Secreted.
Protein Families
Alpha/beta interferon family
Database Links
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