Product Name
msh homeobox 2 (MSX2), ELISA Kit
Full Product Name
Mouse Homeobox protein MSX-2, MSX2 ELISA Kit
Product Synonym Names
Mouse Homeobox protein MSX-2 (MSX2) ELISA kit; CRS2; FPP; HOX8; MSH; PFM; PFM1; msh homeo box 2; msh homeobox homolog 2; msh homeobox 2
Product Gene Name
MSX2 elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
3D Structure
ModBase 3D Structure for Q03358
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of MSX2 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for MSX2 purchase
MBS9333244 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the msh homeobox 2 (MSX2) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing MSX2. The ELISA analytical biochemical technique of the MBS9333244 kit is based on MSX2 antibody-MSX2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect MSX2 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, MSX2. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for MSX2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_038629.2
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NCBI GenBank Nucleotide #
NM_013601.2
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UniProt Primary Accession #
Q03358
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UniProt Secondary Accession #
Q63856[Other Products]
UniProt Related Accession #
Q03358[Other Products]
Molecular Weight
28,915 Da
NCBI Official Full Name
homeobox protein MSX-2
NCBI Official Synonym Full Names
msh homeobox 2
NCBI Official Symbol
Msx2??[Similar Products]
NCBI Official Synonym Symbols
Hox8; Hox-8; Hox8.1; BB122635
??[Similar Products]
NCBI Protein Information
homeobox protein MSX-2; homeobox, msh-like 2; homeo box, msh-like 2; homeobox protein Hox-8-1
UniProt Protein Name
Homeobox protein MSX-2
UniProt Synonym Protein Names
Homeobox protein Hox-8-1
Protein Family
Homeobox protein
UniProt Gene Name
Msx2??[Similar Products]
UniProt Synonym Gene Names
Hox-8.1; Msx-2??[Similar Products]
UniProt Entry Name
MSX2_MOUSE
UniProt Comments for MSX2
MSX2: Acts as a transcriptional regulator in bone development. Represses the ALPL promoter activity and antogonizes the stimulatory effect of DLX5 on ALPL expression during osteoblast differentiation. Probable morphogenetic role. May play a role in limb-pattern formation. In osteoblasts, suppresses transcription driven by the osteocalcin FGF response element (OCFRE). Binds to the homeodomain-response element of the ALPL promoter. Defects in MSX2 are the cause of parietal foramina 1 (PFM1); also known as foramina parietalia permagna (FPP). PFM1 is an autosomal dominant disease characterized by oval defects of the parietal bones caused by deficient ossification around the parietal notch, which is normally obliterated during the fifth fetal month. Defects in MSX2 are the cause of parietal foramina with cleidocranial dysplasia (PFMCCD); also known as cleidocranial dysplasia with parietal foramina. PFMCCD combines skull defects in the form of enlarged parietal foramina and deficient ossification of the clavicles. Defects in MSX2 are the cause of craniosynostosis type 2 (CRS2); also known as craniosynostosis Boston-type (CSB). CRS2 is an autosomal dominant disorder characterized by the premature fusion of calvarial sutures. The craniosynostosis phenotype is either fronto-orbital recession, or frontal bossing, or turribrachycephaly, or cloverleaf skull. Associated features include severe headache, high incidence of visual problems (myopia or hyperopia), and short first metatarsals. Intelligence is normal. Belongs to the Msh homeobox family.
Protein type: Transcription, coactivator/corepressor; DNA-binding
Cellular Component: transcription factor complex; nucleus
Molecular Function: protein binding; DNA binding; sequence-specific DNA binding; transcription cofactor activity; transcription factor binding
Biological Process: embryonic forelimb morphogenesis; transcription from RNA polymerase II promoter; wound healing; positive regulation of apoptosis; multicellular organismal development; negative regulation of transcription from RNA polymerase II promoter; embryonic hindlimb morphogenesis; regulation of apoptosis; anterior/posterior pattern formation; BMP signaling pathway; odontogenesis; negative regulation of cell proliferation; regulation of transcription, DNA-dependent; positive regulation of BMP signaling pathway; embryonic limb morphogenesis; ossification; transcription, DNA-dependent; negative regulation of keratinocyte differentiation; chondrocyte development; stem cell differentiation; negative regulation of fat cell differentiation; positive regulation of catagen; osteoblast development; osteoblast differentiation; regulation of transcription from RNA polymerase II promoter; positive regulation of osteoblast differentiation; cartilage development; embryonic digit morphogenesis; anagen; inhibition of CREB transcription factor; negative regulation of transcription, DNA-dependent; negative regulation of apoptosis; wound healing, spreading of epidermal cells
Research Articles on MSX2
1. Msx1 and Msx2 proteins activate Atoh1 transcription by specifically interacting with several homeodomain s in the Atoh1 3' enhancer.
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