Your Good Partner in Biology Research

  1. 首页
  2. 试剂盒
  3. 酶联免疫试剂盒
  4. Mouse PR domain zinc finger protein 16(PRDM16) ELISA kit

Mouse PR domain zinc finger protein 16(PRDM16) ELISA kit

  • 中文名称：
    小鼠PR结构域锌指蛋白16(PRDM16)酶联免疫试剂盒
  • 货号：
    CSB-EL018645MO
  • 规格：
    96T/48T
  • 价格：
    ￥3600/￥2500
  • 其他：

产品详情

  • 产品描述：

    This Mouse PRDM16 ELISA Kit was designed for the quantitative measurement of Mouse PRDM16 protein in serum, plasma, tissue homogenates, cell lysates. It is a Sandwich ELISA kit, its detection range is 15.6 pg/mL-1000 pg/mL and the sensitivity is 3.9 pg/mL.

  • 别名：
    Prdm16 ELISA Kit; Kiaa1675 ELISA Kit; Mel1Histone-lysine N-methyltransferase PRDM16 ELISA Kit; EC 2.1.1.- ELISA Kit; PR domain zinc finger protein 16 ELISA Kit; PR domain-containing protein 16 ELISA Kit; Transcription factor MEL1 ELISA Kit; MDS1/EVI1-like gene 1 ELISA Kit
  • 缩写：
    PRDM16
  • Uniprot No.：
  • 种属：
    Mus musculus (Mouse)
  • 样本类型：
    serum, plasma, tissue homogenates, cell lysates
  • 检测范围：
    15.6 pg/mL-1000 pg/mL
  • 灵敏度：
    3.9 pg/mL
  • 反应时间：
    1-5h
  • 样本体积：
    50-100ul
  • 检测波长：
    450 nm
  • 研究领域：
    Epigenetics and Nuclear Signaling
  • 测定原理：
    quantitative
  • 测定方法：
    Sandwich
  • 精密度：
    Intra-assay Precision (Precision within an assay): CV%<8%
    Three samples of known concentration were tested twenty times on one plate to assess.
    Inter-assay Precision (Precision between assays): CV%<10%
    Three samples of known concentration were tested in twenty assays to assess.
  • 线性度：
    To assess the linearity of the assay, samples were spiked with high concentrations of mouse PRDM16 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
    SampleSerum(n=4)
    1:1Average %93
    Range %89-99
    1:2Average %96
    Range %91-106
    1:4Average %93
    Range %89-102
    1:8Average %95
    Range %84-98
  • 回收率：
    The recovery of mouse PRDM16 spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.
    Sample TypeAverage % RecoveryRange
    Serum (n=5) 9586-98
    EDTA plasma (n=4)9790-103
  • 标准曲线：
    These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.
    pg/mlOD1OD2AverageCorrected
    10002.651 2.683 2.667 2.469
    5001.944 1.907 1.926 1.728
    2501.093 1.181 1.137 0.939
    1250.744 0.732 0.738 0.540
    62.50.505 0.524 0.515 0.317
    31.20.358 0.367 0.363 0.165
    15.60.277 0.268 0.273 0.075
    00.201 0.195 0.198
  • 数据处理：
  • 货期：
    3-5 working days

产品评价

靶点详情

  • 功能：
    Binds DNA and functions as a transcriptional regulator. Displays histone methyltransferase activity and monomethylates 'Lys-9' of histone H3 (H3K9me1) in vitro. Probably catalyzes the monomethylation of free histone H3 in the cytoplasm which is then transported to the nucleus and incorporated into nucleosomes where SUV39H methyltransferases use it as a substrate to catalyze histone H3 'Lys-9' trimethylation. Likely to be one of the primary histone methyltransferases along with MECOM/PRDM3 that direct cytoplasmic H3K9me1 methylation. Functions in the differentiation of brown adipose tissue (BAT) which is specialized in dissipating chemical energy in the form of heat in response to cold or excess feeding while white adipose tissue (WAT) is specialized in the storage of excess energy and the control of systemic metabolism. Together with CEBPB, regulates the differentiation of myoblastic precursors into brown adipose cells. Functions as a repressor of TGF-beta signaling.
  • 基因功能参考文献：
    1. It is a key factor that induces the differentiation of skeletal muscle precursors to brown adipocytes and simultaneously inhibits myogenic differentiation. PMID: 30097922
    2. Study in mice shows that after 24 h of food deprivation, subcutaneous inguinal white fat takes on many of the morphological and molecular characteristics of visceral fat to preserve energy via miR-149-3p-mediated suppression of PRDM16. PMID: 27240637
    3. PexRAP also interacts with PPARgamma, as well as PRDM16, a critical transcriptional regulator of thermogenesis, and disrupts the PRDM16-PPARgamma complex, providing a potential mechanism for PexRAP-mediated inhibition of adipocyte browning. PMID: 28930673
    4. Consecutive breeding to Flpe and Emx1(IREScre) deleter mice spatially restricted Prdm16 loss to regions of the forebrain expressing the homeobox gene Emx1. PMID: 28424158
    5. Prdm16 interacts with the transcription factor Hlx, which is stabilized in response to beta3-adrenergic signaling, to increase thermogenic gene expression and mitochondrial biogenesis in subcutaneous WAT. PMID: 28701693
    6. Prdm16 is required for adult neural stem cell maintenance and neurogenesis as well as the formation of ependymal cells PMID: 28698301
    7. A single subtype of ganglion cell appears to be uniquely marked by Prdm16 expression. While the precise identity of these ganglion cells is unclear, they most resemble the G9 subtype described by Volgyi and colleagues in 2009. PMID: 29053761
    8. Gelidium elegans stimulates the expression of PRDM16 and UCP-1 Protein in brown adipose tissue and suppresses hyperglycemia in high-fat diet mice. PMID: 28358328
    9. Prdm16 plays an important role in dynamic cellular redox changes in developing neocortex during neural differentiation. PMID: 27993981
    10. Together, these data indicate that PRDM16 diminishes responsiveness to type I interferon in adipose cells to promote thermogenic and mitochondrial function. PMID: 28408438
    11. the cellular levels of alpha-ketoglutarate (alphaKG), a key metabolite required for TET-mediated DNA demethylation, were profoundly increased and required for active DNA demethylation of the Prdm16 promoter. PMID: 27641099
    12. We further show that Cdkn1c is required for post-transcriptional accumulation of the brown fat determinant PR domain containing 16 (PRDM16) and that CDKN1C and PRDM16 co-localise to the nucleus of rare label-retaining cell within iBAT. PMID: 26963625
    13. PRDM16-induced C2C12 transdifferentiation is associated with alterations in CpG methylation of myogenic factors, and PR domain affects both myogenesis and adipogenesis with modified histone methylation marks on MyoD and PPARgamma promoters PMID: 26071185
    14. PRDM16 deficiency in BAT reduces MED1 binding at PRDM16 target sites and causes a fundamental change in chromatin architecture at key brown fat-selective genes PMID: 25644604
    15. Prdm16 and Prdm3 control postnatal BAT identity and function. PMID: 24703692
    16. Study reveals that Prdm16 expression is regulated through Gcn5/PCAF during brown adipogenesis. PMID: 25071153
    17. these studies define the transcriptional pathways involved in HOXB4 HSC expansion in vivo and identify repression of Prdm16 transcription as a mechanism by which expanding HSCs avoid leukemic transformation. PMID: 25082879
    18. miR-133 links to energy balance through targeting Prdm16. PMID: 24085747
    19. These findings indicate that PRDM16 and beige adipocytes are required for the "browning" of white fat and the healthful effects of subcutaneous adipose tissue. PMID: 24439384
    20. adult satellite cells give rise to brown adipocytes and that microRNA-133 regulates the choice between myogenic and brown adipose determination by targeting the 3'UTR of Prdm16. PMID: 23395168
    21. When expressed at elevated levels in brown fat, TLE3 counters Prdm16, suppressing brown-selective genes and inducing white-selective genes, resulting in impaired fatty acid oxidation and thermogenesis. PMID: 23473036
    22. These data suggest that one function of Prdm16 is the regulation of genes that play a role in the differentiation of mesenchymal cells into chondro-/osteocytes. PMID: 23149718
    23. Data indicate that FOS, SPI1, KLF10, TFEC, and PRDM16 show robust transcriptional cross-regulation and are often associated with osteoclastogenesis. PMID: 23340137
    24. Results point to Mef2 and miR-133 as central upstream regulators of Prdm16 and hence of brown adipogenesis in response to cold exposure in BAT and SAT. PMID: 23143398
    25. These results provide the first in vivo evidence that a myogenic regulator together with a growth factor act simultaneously but through independent pathways to repress Prdm16, which opens potential therapeutic perspectives for human metabolic disorders. PMID: 22859371
    26. Data identify Prdm3 and Prdm16 as H3K9me1 methyltransferases and expose a functional framework in which anchoring to the nuclear periphery helps maintain the integrity of mammalian heterochromatin. PMID: 22939622
    27. These results suggest that PRDM16 may play a role in differentiation of mesenchymal cells in the embryonic secondary palate that contribute to the anterior, bony palate and posterior, muscular palate. PMID: 22522345
    28. Results suggest that PPARalpha acts as a key component of brown fat thermogenesis by coordinately regulating lipid catabolism and thermogenic gene expression via induction of PGC-1alpha and PRDM16. PMID: 22033933
    29. These observations identify a novel regulatory axis that includes PPARs, Prdm16, and TGF-beta2 in hematopoiesis. PMID: 21967974
    30. The studies are the first to characterize the expression of the PRDM16 gene during early murine development. PMID: 19853285
    31. Prdm16 integrates hematopoietic stem cell renewal, quiescence, apoptosis, and differentiation PMID: 21343612
    32. Prdm16, a brown adipose determination factor, is selectively expressed in subcutaneous white adipocytes relative to other white fat depots. PMID: 21123942
    33. Prdm16 therefore promotes stem cell maintenance in multiple tissues, partly by modulating oxidative stress. PMID: 20835244
    34. Prdm16 is required for normal palatogenesis in mice PMID: 20007998
    35. PRDM16/MEL1 is a Smad binding protein that may be important for development of orofacial structures through modulation of the TGFbeta signaling pathway. PMID: 17467076
    36. overexpression of sPRDM16 induces abnormal growth of stem cells and progenitors and cooperates with disruption of the p53 pathway in the induction of myeloid leukemia. PMID: 18037989
    37. The regulated docking of the CtBP proteins on PRDM16 controls the brown and white fat-selective gene programs. PMID: 18483224
    38. observed leukemic progression of six distinct clones harboring gamma-retroviral long terminal repeat or SIN vector insertions in Evi1 or Prdm16, two functionally related genes PMID: 18496560
    39. PRDM16 specifies the brown fat lineage from a progenitor that expresses myoblast markers and is not involved in white adipogenesis PMID: 18719582
    40. PRDM16 controls a bidirectional cell fate switch between skeletal myoblasts and brown adipocytes. PMID: 19285866
    41. Prdm16 controls a brown fat/skeletal muscle switch PMID: 18719582

    显示更多

    收起更多

  • 亚细胞定位：
    Nucleus. Cytoplasm.
  • 组织特异性：
    Enriched in BAT compared to WAT. Detected in heart, lung, kidney and brain. Expressed in nuclei of cardiomyocytes.
  • 数据库链接：