Recombinant Mouse CCAAT/enhancer-binding protein beta(Cebpb)

Code CSB-YP005181MO
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Source Yeast
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Code CSB-EP005181MO
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Source E.coli
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Code CSB-EP005181MO-B
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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-BP005181MO
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Source Baculovirus
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Code CSB-MP005181MO
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Source Mammalian cell
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Product Details

Purity >85% (SDS-PAGE)
Target Names Cebpb
Uniprot No. P28033
Alternative Names CebpbCCAAT/enhancer-binding protein beta; C/EBP beta; AGP/EBP; Interleukin-6-dependent-binding protein; IL-6DBP; Liver-enriched transcriptional activator; LAP
Species Mus musculus (Mouse)
Expression Region 1-296
Target Protein Sequence MHRLLAWDAA CLPPPPAAFR PMEVANFYYE PDCLAYGAKA ARAAPRAPAA EPAIGEHERA IDFSPYLEPL APAADFAAPA PAHHDFLSDL FADDYGAKPS KKPADYGYVS LGRAGAKAAP PACFPPPPPA ALKAEPGFEP ADCKRADDAP AMAAGFPFAL RAYLGYQATP SGSSGSLSTS SSSSPPGTPS PADAKAAPAA CFAGPPAAPA KAKAKKTVDK LSDEYKMRRE RNNIAVRKSR DKAKMRNLET QHKVLELTAE NERLQKKVEQ LSRELSTLRN LFKQLPEPLL ASAGHC
Protein Length Full length protein
Tag Info The following tags are available.
N-terminal His-tagged
Tag-Free
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
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
Protein FAQs
Storage Condition Store at -20°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.

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Target Background

Function
(From Uniprot)
Important transcription factor regulating the expression of genes involved in immune and inflammatory responses
Gene References into Functions
  1. findings support that C/EBPbeta plays a pivotal role in AD pathogenesis via increasing delta-secretase expression PMID: 29725016
  2. LCoR negatively regulates early adipogenesis by repressing C/EBP beta transcriptional activity and add LCoR to the growing list of transcriptional corepressors of adipogenesis. PMID: 28972158
  3. results support a stimulatory effect of Pb on adipogenesis which involves ERK activation and C/EBPbeta upregulation prior to PPARgamma and adipogenesis activation. PMID: 28646352
  4. Purple sweet potato colour, a class of naturally occurring anthocyanins, exhibited beneficial effects on hepatic steatosis, which were associated with blocking Src and C/EBPbeta activation. PMID: 28636830
  5. Thus, this study identifies BCL11B as a novel regulator of adipogenesis, which works, at least in part, by stimulating C/EBPbeta activity and suppressing the Wnt/beta-catenin signaling pathway. PMID: 27586877
  6. Study shows that alpha melanocyte stimulating hormone and forkhead box C2 protein promote fatty acid oxidation through C/EBPbeta negative transcription in mice adipose tissue. PMID: 27819350
  7. The results indicated that miR-16 was transactivated by C/EBP-beta resulting in aggravated Ischemia-reperfusion induced acute kidney injury and that urinary miR-16 may serve as a potential biomarker for acute kidney injury. PMID: 27297958
  8. These results suggest that C/EBPbeta is an endogenous initiator of neuropathic pain and could be a potential target for the prevention and treatment of this disorder. PMID: 28698219
  9. We found that C/EBPbeta is phosphorylated by CK2 under AMPK suppression and ER stress, which are important from the viewpoint of the worsening pathological condition of type 2 diabetes, such as decreased insulin secretion and apoptosis of pancreatic beta cells. PMID: 29448105
  10. Expression of the SENP2 gene was suppressed by theobromine. In vivo knockdown studies showed that AR1 knockdown in mice attenuated the anti-adipogenic effects of theobromine in younger mice. Theobromine suppresses adipocyte differentiation and induced C/EBPbeta degradation by increasing its sumoylation. PMID: 28965824
  11. C/EBPbeta is a novel regulator of satellite cell self-renewal during muscle regeneration acting at least in part through Notch2. PMID: 27923399
  12. These data establish C/EBPbeta as a key driver of autoimmune inflammation in EAE, and propose a novel role for C/EBPbeta in regulation of IL-23R expression. PMID: 28088614
  13. C/EBPbeta in hematopoietic cells is crucial to regulate diet-induced inflammation, hyperlipidemia and atherosclerosis development PMID: 27072340
  14. C/EBPbeta or Stat3 depletion by siRNA in sepsis Gr1(+)CD11b(+) MDSCs inhibits miR-21 and miR-181b expression. PMID: 27430527
  15. The present study indicates a requirement for C/EBPbeta in the insulin-mediated induction of SREBP-1c mRNA expression in rodent liver. Coupled with previous data showing that this induction requires LXRalpha, our data reported herein indicate a requirement for both transcription factors. PMID: 27382175
  16. elevated LIP/LAP ratio robustly increased Ogn expression and cell death under stress by modulating the mitogen-activated protein kinase/activator protein 1 pathway (MAPK/AP-1). PMID: 28383550
  17. Ptn may play a vital role in the progesterone-induced decidualization pathway via C/EBPB-cyclic AMP-Hand2 signaling. PMID: 28657144
  18. C/EBPbeta is a critical factor for Ly6C(-) monocyte survival, at least in part through upregulation of Csf1r. PMID: 28807982
  19. these results support that decreasing C/EBPbeta expression prevents MDSC generation and decreases immunosuppression in septic mice, providing a target for sepsis treatment. PMID: 28934717
  20. PARP-1 attenuates adipogenesis by PARylating C/EBPb, a pro-adipogenic transcription factor, on three residues in its regulatory domain. PMID: 28107648
  21. Results show that C/EBPbeta and C/EBPdelta actively regulate the promotor region of both splicing variants Ppargamma1sv and Ppargamma2 in mouse adipocytes. PMID: 23840343
  22. These results show that C/EBPbeta directs a switch from proinflammatory to repressor myeloid cells PMID: 28476751
  23. Both gain- and loss-of-function studies showed that an accumulation of the CCAAT/enhancer binding protein-beta (C/EBP-beta) protein, which cooperates with dominant transcriptional co-regulator PR domain containing 16 (PRDM16) to determine brown/beige adipocyte lineage, is essential for the enhanced adipocyte browning caused by the loss of ZIP13 PMID: 28854265
  24. monocyte differentiation occurred through de novo enhancer establishment and activation of pre-established (poised) enhancers. Generation of Ly6C(-) monocytes involved induction of the transcription factor C/EBPbeta and C/EBPbeta-deficient mice lacked Ly6C(-) monocytes. PMID: 28514690
  25. Intra-tumor IL-6, C/EBP-beta and PPAR-gamma expression correlated with intramuscular liposarcoma growth in mice and autophagy. PMID: 28668397
  26. these findings highlight a critical role of TSC1 in regulating innate immunity by control of the mTOR1-C/EBPbeta pathway. PMID: 27593484
  27. Expression of miR-26a or knockdown of Klf4 or Creb or C/ebpbeta, attenuated the survival of Mycobacterium tuberculosis in macrophages. PMID: 28558034
  28. Valproic acid attenuated muscle wasting and myotube atrophy and reduced C/EBPbeta binding to atrogin1 promoter locus in the myotubes. PMID: 27122162
  29. work shows that helenalin acetate inhibits C/EBPbeta by binding to the N-terminal part of C/EBPbeta, thereby disrupting the cooperation of C/EBPbeta with the co-activator p300. PMID: 27803164
  30. SatM (ceacam1(+)Msr1(+)Ly6C(-)F4/80(-)Mac1(+) monocytes, called "segregated-nucleus-containing atypical monocytes") are critical for fibrosis and C/EBPbeta licenses differentiation of SatM from their committed progenitor PMID: 28002407
  31. The stimulation of CCAAT/enhancer binding protein (C/EBP) beta expression by interleukin-1beta following muscle injury and in cancer cachexia acts to promote muscle satellite cells survival. PMID: 26913600
  32. Cebpb phosphorylation is inhibited by retinoic acid. PMID: 26271478
  33. C/EBPbeta controls M2-macrophage gene expression in the heart. Thus, C/EBPbeta appears as a transcription factor required for cardiac hypertrophy response to gestation. PMID: 26476039
  34. Suggest Hmgn1/Cebpb signaling may play an important role during mouse decidualization. PMID: 26566865
  35. HMGA2 is required for C/EBPbeta-mediated expression of PPAR gamma, and thus promotes adipogenic differentiation. PMID: 26966068
  36. This study showned that the transcription factor C/EBPbeta directly regulates the expression of the C3 gene, and that this control could be relevant for the pro-inflammatory effects of this transcription factor PMID: 25617152
  37. Loss of C/EBPbeta expression in primary myoblasts rescues differentiation under cachectic conditions without restoring myotube size, indicating that C/EBPbeta is an important inhibitor of myogenesis in cancer cachexia. PMID: 26709824
  38. PKR inhibition reduced the expression of eIF4B and C/EBPbeta in an eIF2alpha-independent manner PMID: 26646662
  39. Pharmacologic stimulation of C/EBPbeta expression reprograms myoblasts to a more stem cell-like state, promotes expansion in culture, and improves engraftment such that better transplantation outcomes are achieved. PMID: 26941360
  40. propose that the pathology of MCDS is underpinned by XBP1 independent UPR-induced dysregulation of C/EBP-beta-mediated chondrocyte differentiation PMID: 26372225
  41. C/EBPbeta contributes to immunity to mucosal candidiasis during cortisone immunosuppression in a manner linked to beta-defensin 3 expression, but is apparently dispensable for the IL-17-dependent response. PMID: 26317211
  42. Data suggested that translational adjustment of C/EBPbeta-isoform expression is one of the key processes that direct metabolic adaptation in response to changes in mTORC1 activity. PMID: 26113365
  43. NF-IL6 plays a dual role for sickness response and immune-to-brain communication: acting pro-inflammatory at 8h but anti-inflammatory at 24 h after onset of the inflammatory response reflecting active natural programming of inflammation. PMID: 25813145
  44. Overexpression of LIP significantly reduced the level of polyomavirus JC T-antigen. PMID: 26017382
  45. Par4, CEBPB and FAK form a senescence signaling pathway, playing roles in modulating cell survival, growth, apoptosis, EMT and self-renewal PMID: 25472717
  46. Simulated microgravity activates a p38 MAPK-C/EBPbeta pathway in macrophages to up-regulate arginase and IL-6 expression and down-regulate IL-12B expression PMID: 25804385
  47. C/EBPbeta was the main regulator of P2X7 receptor expression in response to a glucose challenge. C/EBPalpha and the C/EBPbeta-LIP isoform blocked the C/EBPbeta-dependent regulation of P2X7 receptor transcription. PMID: 25403356
  48. C/EBPbeta and RUNX2 cooperatively stimulate expression of Ihh through direct interactions with a C/EBPbeta binding element, which further promotes hypertrophic differentiation of chondrocytes during the chondrocyte differentiation process. PMID: 25105964
  49. Adamts-1 upregulation by inducers of pathological vascular remodeling is mediated by specific signal transduction pathways involving NFAT or C/EBPbeta transcription factors. PMID: 26217013
  50. C/EBPbeta controls lymphoma-associated dendritic cell cytokine expression. PMID: 25266931

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Subcellular Location Nucleus, Cytoplasm
Protein Families BZIP family, C/EBP subfamily
Tissue Specificity Abundantly expressed in myoblasts. Enriched in brown adipose tissue (BAT) versus white adipose tissue (WAT). Expressed in hepatocytes (at protein level). Expressed in T lymphocytes (PubMed:16585579). The expression in granulosa cells of antral follicles i
Database Links

KEGG: mmu:12608

STRING: 10090.ENSMUSP00000069850

UniGene: Mm.439656

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