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  4. Recombinant Human LIM homeobox transcription factor 1-beta (LMX1B)

Recombinant Human LIM homeobox transcription factor 1-beta (LMX1B)

  • 中文名稱：
    人LMX1B重組蛋白
  • 貨號：
    CSB-YP013019HU
  • 規格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    人LMX1B重組蛋白
  • 貨號：
    CSB-EP013019HU
  • 規格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    人LMX1B重組蛋白
  • 貨號：
    CSB-EP013019HU-B
  • 規格：
  • 來源：
    E.coli
  • 共軛：
    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.

  • 其他：
  • 中文名稱：
    人LMX1B重組蛋白
  • 貨號：
    CSB-BP013019HU
  • 規格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    人LMX1B重組蛋白
  • 貨號：
    CSB-MP013019HU
  • 規格：
  • 來源：
    Mammalian cell
  • 其他：

產品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
    LMX1B
  • Uniprot No.：
  • 別名：
    LIM homeo box transcription factor 1 beta; LIM homeobox transcription factor 1 beta; LIM homeobox transcription factor 1-beta; LIM-homeobox protein 1.2; LIM/homeobox protein 1.2; LIM/homeobox protein LMX1B; LMX 1.2; LMX-1.2; LMX1.2; LMX1B; LMX1B_HUMAN; MGC138325; MGC142051; NPS 1; NPS1
  • 種屬：
    Homo sapiens (Human)
  • 蛋白長度：
    Full length protein
  • 表達區域：
    1-402
  • 氨基酸序列
    MDIATGPESL ERCFPRGQTD CAKMLDGIKM EEHALRPGPA TLGVLLGSDC PHPAVCEGCQ RPISDRFLMR VNESSWHEEC LQCAACQQAL TTSCYFRDRK LYCKQDYQQL FAAKCSGCME KIAPTEFVMR ALECVYHLGC FCCCVCERQL RKGDEFVLKE GQLLCKGDYE KEKDLLSSVS PDESDSVKSE DEDGDMKPAK GQGSQSKGSG DDGKDPRRPK RPRTILTTQQ RRAFKASFEV SSKPCRKVRE TLAAETGLSV RVVQVWFQNQ RAKMKKLARR HQQQQEQQNS QRLGQEVLSS RMEGMMASYT PLAPPQQQIV AMEQSPYGSS DPFQQGLTPP QMPGDHMNPY GNDSIFHDID SDTSLTSLSD CFLGSSDVGS LQARVGNPID RLYSMQSSYF AS
  • 蛋白標簽：
    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.
  • 產品提供形式：
    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.
  • 復溶：
    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.
  • 儲存條件：
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質期：
    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.
  • 貨期：
    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.
  • 注意事項：
    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.

產品評價

靶點詳情

  • 功能：
    Essential for the specification of dorsal limb fate at both the zeugopodal and autopodal levels.
  • 基因功能參考文獻：
    1. Study reports two additional families with 18 affected individuals with nail patella-like renal disease (NPLRD). The predominant LMX1B mutation is the previously reported R246Q mutation. PMID: 28059119
    2. Study identified a novel heterozygous in-frame indel mutation of LMX1B in a family of Nail patella syndrome. PMID: 29290531
    3. 9q33.3q34.11 microdeletion including LMX1b gene identified in four patients with intellectual disability, epilepsy, nail dysplasia and bone malformations. PMID: 26395556
    4. Report progression of autosomal dominant renal-limited disease with LMX1B mutation. PMID: 26560070
    5. 38 different LMX1B polymorphisms have been found in 55 families with Nail-Patella Syndrome raising the hypothesis of a genetic heterogeneity. PMID: 25898926
    6. these results reveal a sustained and essential requirement of Lmx1b for the function of midbrain dopamine neurons PMID: 25915474
    7. A heterozygous microdeletion of the entire LMX1B gene using multiplex ligation-dependent probe amplification (MLPA) in a Chinese family with nail patella syndrome, is reported. PMID: 25380522
    8. Results demonstrate that loss of function may not be the only way that mutated LMX1b causes haploinsufficiency. Mutated LMX1b may interfere withdownsteam transcription events. PMID: 24720768
    9. In a large family with the two disorders with two novel frameshift TSC1 and LMX1B mutations, we describe the phenotypes PMID: 24477276
    10. LMX1B is a novel oncogene in ovarian cancer pathogenesis. PMID: 24056967
    11. this study identified two novel mutations of the LMX1B gene in three unrelated families with autosomaldominant Focal Segmental Glomerulosclerosis and no extrarenal features. PMID: 23687361
    12. LMX1B is important in regulating type IV collagen gene expression in the GBM of the developing kidney and also has a likely role in regulating additional genes important in podocyte function and maintenance PMID: 23046462
    13. Data report on the association of LMX1B with autism, though it should be viewed with some caution considering the modest associations we report. PMID: 21901133
    14. c.194 A>C (Q65P) mutation is present in the LMX1B gene of the Chilean patients with nail-patella syndrome associated with glaucoma. PMID: 21850167
    15. effect of lmx1b on gene expression regulation in the brain PMID: 21246047
    16. The co-occurrence of nail-patella syndrome, attention deficit hyperactivity disorder and major depressive disorder may be related to mesencephalic dopaminergic neurologic pathway abnormalities that are a consequence of LMX1B loss of function. PMID: 21184584
    17. Genetic variation in LMX1B may increase the risk of developing schizophrenia. PMID: 20570600
    18. LMX1B mutations is associated with Nail-Patella syndrome. PMID: 20531206
    19. novel mutations in patients with nail patella syndrome PMID: 11668639
    20. Transcriptional induction of slit diaphragm genes by Lmx1b is required in podocyte differentiation. PMID: 11956244
    21. The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes PMID: 11956245
    22. Review. Lmx1b is a homeodomain transcription factor required for glomerular basement membrane collagen expression by podocytes. Its absence in nail-patella syndrome causes abnormalities in many organ systems. PMID: 11978876
    23. LMX1B 17-bp deletion and A3243G mtDNA transition in a previously described PMID: 12646768
    24. These findings indicate that heterozygous mutations of LMX1B do not appear to dramatically affect the expression of type IV collagen chains, podocin, or CD2AP in nail-patella syndrome patients. PMID: 12819019
    25. Single nucleotide polymorphisms in LMX1B gene is associated with nail dysplasia in the nail patella syndrome PMID: 15638822
    26. This is the first study indicating that family history of nephropathy and mutation location might be important in precipitating individual risks for developing NPS renal disease PMID: 15928687
    27. Pathogenic mechanism resulting from the mutation is presumably haploinsufficiency rather than a dominant negative effect, which would explain the clinical variability in this family. PMID: 17515884
    28. familial Mediterranean fever (FMF) heterozygote mutation and nail-patella syndrome (NPS) in 3 members of a family with no pathologic mutation in the LMX1B gene PMID: 17710881
    29. The detection of two entire LMX1B gene deletions and one smaller exonic LMX1B deletion by multiplex ligation-dependent probe amplification (MLPA), is described. PMID: 18414507
    30. study reports a novel LMX1B gene mutation c.368_369delTG, p.C123X in a Japanese girl with the typical nail changes of nail-patella syndrome; the proband's father carried the same mutation, although his fingernails were intact PMID: 18562181
    31. a mutation in the LMX1B gene causes nail-patella syndrome in a Chinese population PMID: 18595794
    32. Familial, genetic proved ((missense mutation -G599A (R200Q)of LMX1B gene))of nail patella syndrome in a mother and her son PMID: 18634531
    33. LMX1B haplotypes influence susceptibility to glaucoma in the general population, suggesting altered LMX1B function predisposes to glaucomatous damage and that this role may be independent of raised intraocular pressure. PMID: 18952915
    34. These data demonstrate for the first time that LMX1B directly regulates transcription of a subset of NF-kappaB target genes in cooperation with nuclear p50/p65 NF-kappaB. PMID: 18996370
    35. podocin is specifically regulated by the transcription factor Lmx1b and by the functional polymorphism -116C/T. PMID: 19562271
    36. A synonymous genetic alteration of LMX1B in a family with nail-patella syndrome. PMID: 19721866

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  • 相關疾病：
    Nail-patella syndrome (NPS)
  • 亞細胞定位：
    Nucleus.
  • 組織特異性：
    Expressed in most tissues. Highest levels in testis, thyroid, duodenum, skeletal muscle, and pancreatic islets.
  • 數據庫鏈接：

    HGNC: 6654

    OMIM: 161200

    KEGG: hsa:4010

    STRING: 9606.ENSP00000347684

    UniGene: Hs.129133



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