Catalog No.
YHD79101
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Ala2-Thr303
Predicted molecular weight
47.12 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P28360
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
Homeobox protein MSX-1, Homeobox protein Hox-7, Msh homeobox 1-like protein, MSX1, HOX7
SK4 potentially modulates the alternative splicing profile associated with papillary thyroid cancer development in BHT101 cells., PMID:40452939
Genetic Aspects of Tooth Agenesis., PMID:40428404
Multidimensional Evidence Chain of Nutritional Impact on Digestive System Tumors: Integration of Mendelian Randomization Causal Inference, NHANES Epidemiological Data, and Transcriptomic Analysis., PMID:40415396
Effects of Acrylamide on Mouse Implantation and Decidualization., PMID:40362368
The dominant negative mutation of PAX9 in nonsyndromic tooth agenesis., PMID:40227334
Functional Analyses of SATB2 Variants Reveal Pathogenicity Mechanisms Linked With SATB2-Associated Syndrome., PMID:39887889
Homeobox protein MSX-1 restricts hepatitis B virus by promoting ubiquitin-independent proteasomal degradation of HBx protein., PMID:39883729
Shh signaling directs dorsal ventral patterning in the regenerating X. tropicalis spinal cord., PMID:39855590
PRMT1-methylated MSX1 phase separates to control palate development., PMID:39843447
Novel MSX1 Gene Variants in Chinese Children with Non-Syndromic Tooth Agenesis: A Clinical and Genetic Analysis., PMID:39767847
Msx1-Modified Rat Bone Marrow Mesenchymal Stem Cell Therapy for Rotator Cuff Repair: A Comprehensive Analysis of Tendon-Bone Healing and Cellular Mechanisms., PMID:39739627
The evolution of cephalic fins in manta rays and their relatives: functional evidence for initiation of domain splitting and modulation of the Wnt signaling pathway in the pectoral fin AER of the little skate., PMID:39731200
Transcriptional factor ISL1 regulates palate development by tuning the SHH cascade., PMID:39704783
Colchicine reduces neointima formation and VSMC phenotype transition by modulating SRF-MYOCD activation and autophagy., PMID:39663419
Exploring the genetics, mechanisms, and therapeutic innovations in non-syndromic tooth agenesis., PMID:39657464
Expression of β-catenin and MSX1 proteins during parrot pseudoteeth and goose denticulations and giant filiform papillae's early development., PMID:39637682
Survival prediction in patients with head and neck squamous cell carcinoma and novel mechanistic insights of S100A8/A9., PMID:39546127
Association of selected gene variants with nonsyndromic orofacial clefts in Kuwait., PMID:39442823
EDA Variants Are Responsible for Approximately 90% of Deciduous Tooth Agenesis., PMID:39408781
Extracellular vesicles derived from Msh homeobox 1 (Msx1)-overexpressing mesenchymal stem cells improve digit tip regeneration in an amputee mice model., PMID:39384602
Identification of Gene Regulatory Networks in B-Cell Progenitor Differentiation and Leukemia., PMID:39202339
What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients., PMID:39183201
The concept of onychodermis containing onychofibroblasts has histological (microanatomical), immunohistochemical as well as molecular basis., PMID:39044464
Genome-Wide CRISPR Screen Identifies an NF2-Adherens Junction Mechanistic Dependency for Cardiac Lineage., PMID:38752370
Msx genes delineate a novel molecular map of the developing cerebellar neuroepithelium., PMID:38742226
Orodental malformations associated with human MSX1 sequence variants., PMID:38713117
miR-21-5p-loaded bone mesenchymal stem cell-derived exosomes repair ovarian function in autoimmune premature ovarian insufficiency by targeting MSX1., PMID:38582043
Effect of MSX1 on the cellular function of cardiomyocytes., PMID:38556116
Early embryogenesis in CHDFIDD mouse model reveals facial clefts and altered cranial neurogenesis., PMID:38511331
MSX1+PDGFRAlow limb mesenchyme-like cells as an efficient stem cell source for human cartilage regeneration., PMID:38428414
Analysis of the cytotoxicity and bioactivity of CeraSeal, BioRoot™ and AH Plus® sealers in pre-osteoblast lineage cells., PMID:38389110
Intrahepatic homeobox protein MSX-1 is a novel host restriction factor of hepatitis B virus., PMID:38226815
Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese families., PMID:38069551
A Comprehensive Bioinformatics Approach to Identify Molecular Signatures and Key Pathways for the Huntington Disease., PMID:38033382
MSX1 Gene Polymorphisms in Patients with non-Syndromic Cleft lip and Palate: A Tertiary Care Centre Based Case-Control Study from Central Kerala., PMID:37968856
Osteogenic potential of apical papilla stem cells mediated by platelet-rich fibrin and low-level laser., PMID:37874511
Prenatal and postnatal challenges affect the hypothalamic molecular pathways that regulate hormonal levels., PMID:37851674
The presence of blastocyst within the uteri facilitates lumenal epithelium transformation for implantation via upregulating lysosome proteostasis activity., PMID:37584546
[Measurement and analysis of the crown conical degree of maxillary incisors in patients with congenital tooth agenesis caused by different gene mutations]., PMID:37550043
Influence of N6-methyladenosine (m6A) modification on cell phenotype in Alzheimer's disease., PMID:37549144
Analysis of Angiogenesis-Related Signatures in the Tumor Immune Microenvironment and Identification of Clinical Prognostic Regulators in Lung Adenocarcinoma., PMID:37522541
Association of MSX1 Gene Variants with Nonsyndromic Cleft Lip and/or Palate in the Pakistani Population., PMID:37431261
Genetic analysis of transcription factors in dopaminergic neuronal development in Parkinson's disease., PMID:37341647
Persistence of FoxJ1+ Pax6+ Sox2+ ependymal cells throughout life in the human spinal cord., PMID:37329342
Inflammatory Response and Exosome Biogenesis of Choroid Plexus Organoids Derived from Human Pluripotent Stem Cells., PMID:37108817
MSX1-expression during the different phases in healthy human endometrium., PMID:37101223
Single-cell transcriptome profiling reveals distinct expression patterns among genes in the mouse incisor dental pulp., PMID:37078362
Global Quantitative Proteomics Analysis Reveals the Downstream Signaling Networks of Msx1 and Msx2 in Myoblast Differentiation., PMID:36939786
Correction: Emerin anchors Msx1 and its protein partners at the nuclear periphery to inhibit myogenesis., PMID:36906651
MSX1 Regulates Goat Endometrial Function by Altering the Plasma Membrane Transformation of Endometrial Epithelium Cells during Early Pregnancy., PMID:36835532
For research use only. Not for human or drug use.
