Recombinant Mouse Vitamin D3 receptor (Vdr)

Code CSB-YP025832MO
MSDS
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Source Yeast
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Code CSB-EP025832MO
MSDS
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Source E.coli
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Code CSB-EP025832MO-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-BP025832MO
MSDS
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Source Baculovirus
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Code CSB-MP025832MO
MSDS
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Source Mammalian cell
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Product Details

Purity
>85% (SDS-PAGE)
Target Names
Vdr
Uniprot No.
Alternative Names
Vdr; Nr1i1; Vitamin D3 receptor; VDR; 1,25-dihydroxyvitamin D3 receptor; Nuclear receptor subfamily 1 group I member 1
Species
Mus musculus (Mouse)
Expression Region
1-422
Target Protein Sequence
MEAMAASTSL PDPGDFDRNV PRICGVCGDR ATGFHFNAMT CEGCKGFFRR SMKRKALFTC PFNGDCRITK DNRRHCQACR LKRCVDIGMM KEFILTDEEV QRKREMIMKR KEEEALKDSL RPKLSEEQQH IIAILLDAHH KTYDPTYADF RDFRPPIRAD VSTGSYSPRP TLSFSGDSSS NSDLYTPSLD MMEPASFSTM DLNEEGSDDP SVTLDLSPLS MLPHLADLVS YSIQKVIGFA KMIPGFRDLT SDDQIVLLKS SAIEVIMLRS NQSFTLDDMS WDCGSQDYKY DITDVSRAGH TLELIEPLIK FQVGLKKLNL HEEEHVLLMA ICIVSPDRPG VQDAKLVEAI QDRLSNTLQT YIRCRHPPPG SHQLYAKMIQ KLADLRSLNE EHSKQYRSLS FQPENSMKLT PLVLEVFGNE IS
Protein Length
Full length 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
Nuclear receptor for calcitriol, the active form of vitamin D3 which mediates the action of this vitamin on cells. Enters the nucleus upon vitamin D3 binding where it forms heterodimers with the retinoid X receptor/RXR. The VDR-RXR heterodimers bind to specific response elements on DNA and activate the transcription of vitamin D3-responsive target genes. Plays a central role in calcium homeostasis.
Gene References into Functions
  1. Data suggest that Smad-specific E3 ubiquitin ligase 2 (SMURF2)-mediated SMAD3 protein (SMAD3) monoubiquitination interferes with the formation of a SMAD3-vitamin D receptor (VDR) complex. PMID: 28216630
  2. Vitamin D inhibits lymphangiogenesis through VDR-dependent mechanisms. PMID: 28303937
  3. Data suggests that exposure to vitamin D deficiency during perinatal period directly affects expression of genes involved in development of adipose tissue in non-obese offspring; expression levels of Pparg (peroxisome proliferator activated receptor gamma) and Vdr (vitamin D receptor) are up-regulated in adipose tissue of male offspring. PMID: 28004271
  4. The elevated levels of miR-351 promoted hepatic fibrosis by targeting the vitamin D receptor (VDR), which is an antagonist of SMAD signaling. PMID: 29255036
  5. the crucial role of VDR in anti-inflammatory effects in lungs PMID: 28803336
  6. In murine blood cells 1,25-Dihydroxyvitamin D, but not all-trans-retinoic acid, upregulates the expression of VDR. PMID: 28635660
  7. These findings suggest that the vitamin D treatment-induced increase in bone mass is mediated by suppressing bone resorption through VDR in osteoblast-lineage cells. PMID: 28177161
  8. Gut epithelial VDR signaling controls mucosal inflammation by suppressing epithelial cell apoptosis. PMID: 29228157
  9. Expression of VDR exclusively in the distal intestine can prevent abnormalities in calcium homeostasis and bone mineralization associated with systemic VDR deficiency. PMID: 28938396
  10. Data suggest that the absence of VDR inhibits atherosclerotic plaque calcification in hypercholesterolemic Apoe(-/-) mice, providing additional insight into the role of vitamin D in atherosclerotic plaque calcification. PMID: 27567005
  11. Activated RAS signaling reduced Vitamin D Receptor (VDR) level in intestinal epithelial cells. PMID: 28104492
  12. Loss of the vitamin D receptor in macrophages and granulocytes mildly affected colitis-associated symptoms but greatly increased proinflammatory cytokine expression in the inflamed colon, suggesting a prominent role for innate immune cell vitamin D signaling in controlling gut inflammation. PMID: 28472309
  13. Unique protective roles for vitamin D signaling during colitis in the colon epithelium as well as nonepithelial cells in the colon microenvironment (i.e., modulation of M biology). PMID: 28368514
  14. Vdr and Casr are required for beta-catenin-regulated cell proliferation and Adherens junction formation essential for re-epithelialization after wounding. Vitamin D and calcium signaling in keratinocytes are required for a normal regenerative response of the skin to wounding. PMID: 28368538
  15. Absence of VDR-mediated PPARgamma suppression underlies alopecia in VDR-/- mice. PMID: 27932380
  16. Through the VDR, vitamin D is an environmental factor that helps to maintain low serum IgE responses. PMID: 28003380
  17. VDR is important for the maintenance of physiological level of Axin1 PMID: 27601169
  18. The data support the hypothesis that Vdr in mature adipocytes alters the metabolic response to high-fat diets and exerts anti-proliferative effects on the mammary epithelium. PMID: 26429395
  19. The data demonstrate that deficiency in the vitamin D signaling via VDR knockout enhances the pathological phenotype in this experimental cardiomyopathy and suggest an important role for vitamin D in modulating disease severity in common cardiovascular disorders. PMID: 26429397
  20. Absence of VDR or presence of an unliganded VDR does not affect the profile and function of ex vivo generated bone marrow-derived dendritic cells. PMID: 26343449
  21. JNK1 physically and functionally interacted with VDR and positively regulated VDR expression at transcriptional and translational levels, which influenced calcitriol-mediated inhibition of cancer cell proliferation. PMID: 27174721
  22. Vitamin D receptor activation reduces dissecting abdominal aortic aneurysm formation induced by Ang-II in apoE(-/-) mice PMID: 27283745
  23. VDR may function as a selective suppressor/de-repressor of gene expression in the absence of 1,25-dihydroxyvitamin D3. PMID: 26323657
  24. In the presence of normocalcemia, absence of VDR or its ligand-activated transcription of genes has no direct regulatory effect on murine glucose homeostasis or gene expression in islets of Langerhans. PMID: 26877201
  25. The Vdr-/- mouse model displays sex- and site-specific differences in skeletal structures with long-term feeding of a rescue diet. PMID: 26690785
  26. The endothelial cell VDR plays a tonic inhibitory role in regulating glucose disposal and could prove to be a factor in controlling glucose homeostasis in the intact organism. PMID: 26369613
  27. Cyp27b1(-/-) mice exhibited hypocalcemia, growth defects, and skeletogenesis dysfunction, similar to Vdr(-/-) mice, but do not display alopecia PMID: 28025137
  28. expression in macrophages is essential for the normal expansion of tissue-resident macrophages in response to cutaneous wounding PMID: 27526034
  29. Collectively, we identify a novel regulatory pathway in which 1, 25(OH)2D3 induces VDR expression and promotes VDR interaction with p50 subunit of NF-kappaB, which in turn attenuates the association of KLF5 with p50 subunit of NF-kappaB and thus exerts anti-inflammatory and anti-proliferative effects on macrophages. PMID: 27856242
  30. there was a positive correlation between VDR status and the expression of Suppressor of fused gene (SuFu), a hedgehog pathway inhibitor. miR-214 on the other hand suppressed SuFu protein expression. PMID: 27693451
  31. Vitamin D and its receptor might be involved in the progression of diabetic nephropathy by regulating transforming growth factor-beta, angiotensinogen expression and apoptosis of podocytes. PMID: 27180929
  32. The major finding of this study is that large intestine VDR significantly contributes to whole-body Ca metabolism but that duodenal compensation may prevent the consequences of VDR deletion from large intestine and kidney in growing mice. PMID: 26211511
  33. The present study investigated whether the vitamin D/vitamin D receptor (VDR) pathway may ameliorate lipopolysaccharide (LPS)induced ALI through maintaining the integrity of the alveolar epithelial barrier. PMID: 26675943
  34. Data, including data from studies in knockout mice, suggest that VDR regulates expression of ezrin in enterocytes; however, VDR appears not to be involved in morphology of tight junctions and absorption of large molecules in enterocytes. PMID: 26606857
  35. These data indicate a synergistic crosstalk between 1alpha,25(OH)2D3 and BMP2 toward osteogenesis and mineral deposition, involving both VDR and Pdia3. PMID: 23784946
  36. study is the first to report an in vivo association between vitamin D, myostatin, and the regulation of muscle mass PMID: 26340892
  37. The current study reveals an important and novel mechanism for VDR by regulation of epithelial barriers. PMID: 26212084
  38. VitD3 reinforced physical interaction between placental VDR and NF-kappaB p65 subunit. PMID: 26065916
  39. 1,25D3 modulates CD8+ T cell phenotype via recruitment of the VDR transcription factor to the promoter region of Cyp11a1 leading to prevention of lung allergic responses. PMID: 26750596
  40. Data (including data from studies in knockout mice) suggest signal transduction via calcitriol/calcitriol receptor regulates expression of Elovl3 (fatty acid elongase 3) and alters fatty acid composition in subcutaneous (not visceral) adipose tissue. PMID: 26488808
  41. Absent immune cell VDR expression does not impact the strength/phenotype/linetics of heart transplant rejection in mice and does not impact the graft-prolonging effects of costimulatory blockade including that induced by clinically used CTLA4Ig. PMID: 25719262
  42. these studies delineate a protective role for vitamin D receptor signaling in Ron-induced mammary tumorigenesis through disruption of beta-catenin activation. PMID: 26008979
  43. These studies define mechanisms associated with hormonal regulation of the Vdr and hint at the differential nature of VDR binding activity at the Vdr gene in different primary target tissues in vivo. PMID: 26504088
  44. VDR expression is lost in the majority of the colon tumor cells. PMID: 25873367
  45. cross-talk between the maternal decidua and the placenta, as well as maternal vitamin D status, may be more important in determining pregnancy outcome than conceptus expression of VDR. PMID: 26121239
  46. Dysbiosis caused by vitamin D receptor deficiency confers colonization resistance to Citrobacter rodentium through modulation of innate lymphoid cells. PMID: 25315967
  47. Our findings show a direct, VDR-mediated, protective effect of 1,25(OH) )2D3 against ischemic injury-induced blood-brain barrier dysfunction in cerebral endothelial cells PMID: 25815722
  48. PPARgamma was also decreased upon treatment with VDR siRNA. The above results demonstrate that active vitamin D promoted M1 phenotype switching to M2 via the VDR-PPARg pathway. PMID: 25961000
  49. Myeloid VDR deletion enables M2 monocytes to transport cholesterol into atherosclerotic plaques. PMID: 25801026
  50. VDR is a novel endogenous self-defensive and cardioprotective receptor against myocardial ischemia/reperfusion injury, via mechanisms (at least in part) reducing oxidative stress, and inhibiting apoptosis and autophagy. PMID: 25365634

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Subcellular Location
Nucleus. Cytoplasm.
Protein Families
Nuclear hormone receptor family, NR1 subfamily
Database Links
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