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Browse our anti-MSX1 (MSX1) Antibodies

Full name:
anti-Msh Homeobox 1 Antibodies (MSX1)
On are 106 Msh Homeobox 1 (MSX1) Antibodies from 20 different suppliers available. Additionally we are shipping MSX1 Proteins (18) and MSX1 Kits (4) and many more products for this protein. A total of 141 MSX1 products are currently listed.
AA675338, AI324650, CHOX-7, ECTD3, GHOX-7, HOX-7, Hox7, Hox7.1, HYD1, msh, STHAG1
list all antibodies Gene Name GeneID UniProt
MSX1 4487 P28360
MSX1 17701 P13297
MSX1 81710  

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Most Popular Reactivities for anti-MSX1 (MSX1) Antibodies

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anti-Human MSX1 Antibodies:

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Top referenced anti-MSX1 Antibodies

  1. Human Polyclonal MSX1 Primary Antibody for DB, EIA - ABIN493137 : Davidson: The function and evolution of Msx genes: pointers and paradoxes. in Trends in genetics : TIG 1995 (PubMed)
    Show all 4 references for ABIN493137

  2. Human Monoclonal MSX1 Primary Antibody for EIA, WB - ABIN1108305 : Li, Cui, Fang, Mei: [A novel mutation of MSX1 gene in a Chinese pedigree with oligodontia]. in Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology 2008 (PubMed)
    Show all 2 references for ABIN1108305

  3. Dog (Canine) Polyclonal MSX1 Primary Antibody for WB - ABIN2779956 : Lee, Andersen, Cabernard, Manning, Tran, Lanskey, Bashirullah, Doe: Drosophila Aurora-A kinase inhibits neuroblast self-renewal by regulating aPKC/Numb cortical polarity and spindle orientation. in Genes & development 2006 (PubMed)
    Show all 2 references for ABIN2779956

  4. Human Monoclonal MSX1 Primary Antibody for ELISA, WB - ABIN969296 : Mizokami, Egashira, Takekoshi, Itoh, Itoh, Osamura, Matsumae: Expression of MSX1 in human normal pituitaries and pituitary adenomas. in Endocrine pathology 2009 (PubMed)
    Show all 2 references for ABIN969296

  5. Dog (Canine) Polyclonal MSX1 Primary Antibody for IHC, WB - ABIN2777275 : Djoussé, Knowlton, Hayden, Almqvist, Brinkman, Ross, Margolis, Rosenblatt, Durr, Dode, Morrison, Novelletto, Frontali, Trent, McCusker, Gómez-Tortosa, Mayo Cabrero, Jones, Zanko, Nance, Abramson, Suchowersky, Paulsen, Harrison, Yang, Cupples, Mysore, Guse: Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. in Neurogenetics 2004 (PubMed)
    Show all 2 references for ABIN2777275

  6. Cow (Bovine) Polyclonal MSX1 Primary Antibody for EIA, IHC (p) - ABIN374442 : Villafranca, Lázaro, Salinas, Garcés: Stimulated Brillouin scattering gain profile characterization by interaction between two narrow-linewidth optical sources. in Optics express 2009 (PubMed)

  7. Human Polyclonal MSX1 Primary Antibody for IHC (p), IHC - ABIN268531 : Blin-Wakkach, Lezot, Ghoul-Mazgar, Hotton, Monteiro, Teillaud, Pibouin, Orestes-Cardoso, Papagerakis, Macdougall, Robert, Berdal: Endogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammals. in Proceedings of the National Academy of Sciences of the United States of America 2001 (PubMed)

  8. Human Polyclonal MSX1 Primary Antibody for FACS, IF (cc) - ABIN1385926 : Mu, Wu, Zhu, Li, Tang, Yao, Yang, Peng, Li, Hua: The function of Msx1 gene in promoting meiosis of dairy goat male germline stem cells (mGSCs). in Cell biochemistry and function 2013 (PubMed)

More Antibodies against MSX1 Interaction Partners

Human Msh Homeobox 1 (MSX1) interaction partners

  1. We found the c.*6C > T variation in the MSX1 gene. This variant in the 3' untranslated region is located 6 bp downstream of the stop codon (TAG) in exon 2. We revealed a statistically significant association between the MSX1 c.*6C > T variant and Nonsyndromic cleft lip/palate in Turkey ( p = 0.01).

  2. The results of this study suggest an association between CL/P susceptibility and SNP1 (show SNRNP70 Antibodies), located near the MSX1 gene, in the Mexican population.

  3. Our study showed that TGFA (show TGFA Antibodies)/TGFB3 (show TGFB3 Antibodies)/MSX1 gene polymorphisms were associated with congenital NSHI. The distribution of genotype frequencies and allele frequencies of TGFA (show TGFA Antibodies) rs3771494, TGFB3 (show TGFB3 Antibodies) rs3917201 and rs2268626, and MSX1 rs3821949 and rs62636562 were significantly different between the case and the control groups

  4. MSX1 was able to inhibit the Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling pathway, and that the ability to regulate the Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling pathway is critical for MSX1 to suppress glioblastoma cell migration and invasion.

  5. mutations in MSX1 gene might play an important role in hypodontia cases involving pre-molars and is a risk factor for this ethnic population mainly of Arabs and is first report linking these mutations with tooth agenesis.

  6. identification and characterization of a novel intronic mutation in the MSX1 gene in a large Chinese pedigree, adding to the small repertoire of MSX1 mutations associated with autosomal dominant tooth agenesis.

  7. study reports 2 novel MSX1 mutations (c.739C>T; p.Pro247Ser and c.607G>A; p.Ala203Thr) in 2 Thai families; one is associated with preaxial polydactyly of the left hand, bilateral cleft lip and palate, hypodontia, microdontia and dens invaginatus; the other is associated with unilateral cleft lip and palate, microdontia and hypodontia

  8. The SNPs rs3821949 and rs12532 in the MSX1 gene were associated with congenital heart diseases in Chinese Han populations.

  9. The sequence dependence of local conformation of DNA enables MSX1 glutamine50>lysine to make hydrogen bond with its target nucleotide(s) of DNA.

  10. a Japanese family with nonsyndromic tooth agenesis caused by a novel nucleotide substitution in the intronic region between exons 1 and 2 of the MSX1 gene, is reported.

Pig (Porcine) Msh Homeobox 1 (MSX1) interaction partners

  1. Msx1 may play a role in repressing gene expression in the fetal and postnatal periods.

Mouse (Murine) Msh Homeobox 1 (MSX1) interaction partners

  1. Data show that the spatiotemporal expression of claudin-1 (show CLDN1 Antibodies) is dysregulated in homeobox (show PRRX1 Antibodies) (Msx) genes Msx1d/d/Msx2d/d uteri.

  2. MSX1 linked the arterial shear stimulus to arteriogenic remodeling by activating the endothelial but not medial layer to a proinflammatory state because EC but not smooth muscle cell

  3. Msx1 and Msx2 are direct transcriptional targets of Lhx2 (show LHX2 Antibodies).

  4. Msx1 appears to act as a modeling factor for membranous bone.

  5. analysis of a BMP signaling pathway that regulates the expression of the odontogenic gene Msx1 and determines the fate of dental mesenchyme during early tooth development

  6. Msx1 supports vascular mineralization by directing the osteogenic programming of aortic progenitors in diabetic arteriosclerosis.

  7. Msx1 and Msx2 proteins activate Atoh1 (show ATOH1 Antibodies) transcription by specifically interacting with several homeodomain binding sites in the Atoh1 (show ATOH1 Antibodies) 3' enhancer.

  8. Study concludes that MSX1 may promote proliferation and prevent the differentiation of dental mesenchymal cells by the inhibition of Bmp2 (show BMP2 Antibodies) and Bmp4 (show BMP4 Antibodies) expression.

  9. Msx1 interacts with Lhx6 (show LHX6 Antibodies) and Sna (show SNAI1 Antibodies) in vivo. A network of transcription factors operates during early tooth morphogenesis.

  10. Msx1 functions as a negative regulator early in pituitary development by repressing the gonadotrope-specific alphaGSU (show CGA Antibodies) and GnRHR (show GNRHR Antibodies) genes.

Cow (Bovine) Msh Homeobox 1 (MSX1) interaction partners

  1. Suppression of MSX1 affects oocyte maturation, embryo cleavage rate, and expression of numerous genes suggesting important role for MSX1 in embryo development.

MSX1 Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with MSX1

  • homeobox protein MSX-1-like (LOC722771) antibody
  • msh homeobox 1 (MSX1) antibody
  • msh homeobox 1 (Msx1) antibody
  • AA675338 antibody
  • AI324650 antibody
  • CHOX-7 antibody
  • ECTD3 antibody
  • GHOX-7 antibody
  • HOX-7 antibody
  • Hox7 antibody
  • Hox7.1 antibody
  • HYD1 antibody
  • msh antibody
  • STHAG1 antibody

Protein level used designations for anti-Msh Homeobox 1 (MSX1) Antibodies

homeobox 7 , homeobox protein Hox-7 , homeobox protein MSX-1 , msh homeo box 1 , msh homeobox 1-like protein , msh homeobox homolog 1 , homeo box, msh-like 1 , homeobox, msh-like 1 , hox-7.1 , muscle-segment homeobox , msh homeo box homolog 1 , Hbox 7 , homeobox protein GHOX-7

722771 Macaca mulatta
4487 Homo sapiens
488828 Canis lupus familiaris
100302364 Sus scrofa
17701 Mus musculus
81710 Rattus norvegicus
286872 Bos taurus
396484 Gallus gallus
461092 Pan troglodytes
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