16366-1-AP targets SHOX2 in WB, IHC, ELISA applications and shows reactivity with human, mouse, rat samples. PBS with 0.02% sodium azide and 50% glycerol pH 7.3. Store at -20°C. …

2024年12月25日 · SHOX2 (SHOX Homeobox 2) is a Protein Coding gene. Diseases associated with SHOX2 include Turner Syndrome and Cornelia De Lange Syndrome. Gene Ontology (GO) annotations related to this gene include sequence-specific DNA binding. An important paralog of this gene is SHOX.

In this study, we found that SHOX2 expression was significantly raised in PCa tissues and was associated with clinicopathological features as well as disease-free survival (DFS) of PCa patients. Phenotypic tests showed that the absence of SHOX2 inhibited PCa growth and invasion, while SHOX2 overexpression promoted these effects.

SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome.

IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.

View Mouse Monoclonal anti-SHOX2 Antibody (1D1) (H00006474-M01). Validated Applications: WB, ELISA, S-ELISA, KD. Validated Species: Human, Rat.

SHOX2 antibody LS-C829288 is an unconjugated rabbit-new zealand white polyclonal antibody to SHOX2 from mouse. It is reactive with human, mouse and rat. Validated for IHC and WB.

2022年6月28日 · We evaluated the diagnostic potential of a SHOX2 and RASSF1A combined promoter methylation assay for detection of early LUAD in the NJDT cohort. Then we explored the promoter methylation levels of SHOX2 and RASSF1A and their gene expression between normal and tumor samples at different stages in both cohorts.