Catalog No.
YHJ12001
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Ser2690-Leu2809
Predicted molecular weight
40.25 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q75N90
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
FBN3, Fibrillin-3, KIAA1776
Genetic Insights into Skeletal Malocclusion: The Role of the FBN3 rs7351083 SNP in the Romanian Population., PMID:39064490
Expression of transforming growth factor β signalling molecules and their correlations with genes in loci linked to polycystic ovary syndrome in human foetal and adult tissues., PMID:38894494
Genetic models of fibrillinopathies., PMID:37972149
Missense polymorphisms potentially involved in mandibular prognathism., PMID:37228872
Co-Expression Analysis of Airway Epithelial Transcriptome in Asthma Patients with Eosinophilic vs. Non-Eosinophilic Airway Infiltration., PMID:36835202
Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet-Biedl Syndrome-Like Phenotype., PMID:35910214
Candidate genes for polycystic ovary syndrome are regulated by TGFβ in the bovine foetal ovary., PMID:35413103
Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified., PMID:35141985
ceRNA network development and tumour-infiltrating immune cell analysis of metastatic breast cancer to bone., PMID:32760644
Analysis of expression of candidate genes for polycystic ovary syndrome in adult and fetal human and fetal bovine ovaries†., PMID:32678441
Identification of clinical trait-related lncRNA and mRNA biomarkers with weighted gene co-expression network analysis as useful tool for personalized medicine in ovarian cancer., PMID:31462944
Transcript abundance of stromal and thecal cell related genes during bovine ovarian development., PMID:30856218
Genetic Factors Involved in Mandibular Prognathism., PMID:28570402
Thyroid disorders in polycystic ovary syndrome., PMID:28165551
Regulation of fibrillins and modulators of TGFβ in fetal bovine and human ovaries., PMID:27222596
Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin., PMID:26752647
BSND and ATP6V1G3: Novel Immunohistochemical Markers for Chromophobe Renal Cell Carcinoma., PMID:26091477
Expression and clinical significance of genes frequently mutated in small cell lung cancers defined by whole exome/RNA sequencing., PMID:25863124
Heparin/heparan sulfate controls fibrillin-1, -2 and -3 self-interactions in microfibril assembly., PMID:25034023
Transcriptional profiling of the human fibrillin/LTBP gene family, key regulators of mesenchymal cell functions., PMID:24703491
Biochemical properties of tissue-engineered cartilage., PMID:24406561
The role of TGF-β in polycystic ovary syndrome., PMID:23585338
Microsatellite polymorphism in the fibrillin 3 gene and susceptibility to PCOS: a case-control study and meta-analysis., PMID:23265956
Genetics of the polycystic ovary syndrome., PMID:23079471
Structure and function of the mammalian fibrillin gene family: implications for human connective tissue diseases., PMID:22921888
Association of fibrillin-3 and transcription factor-7-like 2 gene variants with metabolic phenotypes in PCOS., PMID:22301903
Linkage of regulators of TGF-β activity in the fetal ovary to polycystic ovary syndrome., PMID:21411746
Fibrillin-3 expression in human development., PMID:20970500
Fibrillins in adult human ovary and polycystic ovary syndrome: is fibrillin-3 affected in PCOS?, PMID:20855553
A variant in the fibrillin-3 gene is associated with TGF-β and inhibin B levels in women with polycystic ovary syndrome., PMID:20630504
Family-based analysis of candidate genes for polycystic ovary syndrome., PMID:20200332
Genetic and gene expression analyses of the polycystic ovary syndrome candidate gene fibrillin-3 and other fibrillin family members in human ovaries., PMID:19692420
Fibrillins and latent TGFbeta binding proteins in bovine ovaries of offspring following high or low protein diets during pregnancy of dams., PMID:19524133
[FBN3 gene polymorphisms in adolescent idiopathic scoliosis patients]., PMID:19192405
Identification of a polycystic ovary syndrome susceptibility variant in fibrillin-3 and association with a metabolic phenotype., PMID:17785364
Dietary iron deficiency compromises normal development of elastic fibers in the aorta and lungs of chicks., PMID:17634261
Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients., PMID:15221638
Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues., PMID:14962672
For research use only. Not for human or drug use.
