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MSX1 Matched Antibody Pair (760) (APMAB-760LY)


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Specifications

ApplIcation
Sandwich ELISA
Specificity
Human
Capture Antibody
Mouse anti-MSX1 monoclonal, IgG2a antibody, 100 ug
Detection Antibody
Anti-MSX1 Biotinylated mouse monoclonal, IgG2a antibody, 50 ug
Dilutions
10 ng/ml-100 ng/ml
Format
Liquid
Storage
Aliquot and store at -20°Cor -80°C. Avoid freeze-thaw cycles.
Introduction
This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq, Jul 2008]
Alternative Names
Msh Homeobox 1; Msh Homeobox 1-Like Protein; Homeobox Protein Hox-7; HOX7; Msh (Drosophila) Homeo Box Homolog 1 (Formerly Homeo Box 7); Msh Homeobox Homolog 1 (Drosophila); Homeobox Protein MSX-1;
Entrez Gene ID
4487
UniProt ID
P28360
More Infomation

Zhou, G., Ma, S., Yang, M., & Yang, Y. (2022). Global Quantitative Proteomics Analysis Reveals the Downstream Signaling Networks of Msx1 and Msx2 in Myoblast Differentiation. Phenomics, 2(3), 201-210.

Singh, S., Biswas, S., Srivastava, A., Mishra, Y., & Chaturvedi, T. P. (2021). In silico characterization and structural modeling of a homeobox protein MSX1 from homo sapiens. Informatics in Medicine Unlocked, 22, 100497.

Kwon, D. H., Choe, N., Shin, S., Ryu, J., Kim, N., Eom, G. H., ... & Kook, H. (2021). Regulation of MDM2 E3 ligase-dependent vascular calcification by MSX1/2. Experimental & Molecular Medicine, 53(11), 1781-1791.

Olsson, B., Calixto, R. D., da Silva Machado, N. C., Meger, M. N., Paula-Silva, F. W. G. D., Rebellato, N. L. B., ... & Scariot, R. (2020). MSX1 is differentially expressed in the deepest impacted maxillary third molars. British Journal of Oral and Maxillofacial Surgery, 58(7), 789-794.

Yang, Y., Zhu, X., Jia, X., Hou, W., Zhou, G., Ma, Z., ... & Wang, G. (2020). Phosphorylation of Msx1 promotes cell proliferation through the Fgf9/18-MAPK signaling pathway during embryonic limb development. Nucleic Acids Research, 48(20), 11452-11467.

Horazna, M., Janeckova, L., Svec, J., Babosova, O., Hrckulak, D., Vojtechova, M., ... & Korinek, V. (2019). Msx1 loss suppresses formation of the ectopic crypts developed in the Apc-deficient small intestinal epithelium. Scientific Reports, 9(1), 1629.

Mártha, K., Kerekes Máthé, B., Moldovan, V. G., & Bănescu, C. (2019). Study of rs12532, rs8670 polymorphism of Msh homeobox 1 (MSX1), rs61754301, rs4904155 polymorphism of paired box gene 9 (PAX9), and rs2240308 polymorphism of axis inhibitor protein 2 (AXIN2) genes in nonsyndromic hypodontia. BioMed Research International, 2019.

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For research use only. Not intended for any clinical use.

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