The function of SCML1 remains unknown.
- Known as:
- The function SCML1 remains unknown.
- Catalog number:
- 25-287
- Product Quantity:
- 0.05 mg
- Category:
- -
- Supplier:
- Prosci
- Gene target:
- The function SCML1 remains unknown.
Ask about this productRelated genes to: The function of SCML1 remains unknown.
- Gene:
- SCML1 NIH gene
- Name:
- Scm polycomb group protein like 1
- Previous symbol:
- -
- Synonyms:
- -
- Chromosome:
- Xp22.13
- Locus Type:
- gene with protein product
- Date approved:
- 1997-09-05
- Date modifiied:
- 2017-07-18
Related products to: The function of SCML1 remains unknown.
150 kDa cofactor of initiator function,CIF150,Homo sapiens,Human,RNA polymerase II TBP-associated factor subunit B,TAF(II)150,TAF2,TAF2B,TAFII150,TAFII-150,TBP-associated factor 150 kDa,Transcription17-AAG(Geldanamycin) 17-AAG is a less toxic analogue of the geldanamycin which binds to Hsp90 and alters its function. For research use only.6-Epi Doxycycline, 65% (Contains Unknown Salts) C22H24N2O8 CAS: 3219-99-66-Epi Doxycycline, 65% (Contains Unknown Salts) CAS: 3219-99-6 Formula: C22H24N2O8A single licensed Software Package for control functionA single licensed Software Package for control functionA single licensed Software Package for control function, including a RS 232 CableA single licensed Software Package for control function, including a RS 232 CableA1BG is a plasma glycoprotein of unknown function. It shows sequence similarity to the variable regions of some immunoglobulin supergene family member proteins.A1BG is a plasma glycoprotein of unknown function. It shows sequence similarity to the variable regions of some immunoglobulin supergene family member proteins. The protein encoded by this gene is a pABHD13 is a single-pass type II membrane protein. It belongs to the serine esterase family. The exact function of ABHD13 remains unknown.Western blots using two different antibodies against two uniqueABHD13 is a single-pass type II membrane protein. It belongs to the serine esterase family. The exact function of ABHD13 remains unknown.Western blots using two different antibodies against two uniqueABHD13 is a single-pass type II membrane protein. It belongs to the serine esterase family. The exact function of ABHD13 remains unknown.Western blots using two different antibodies against two uniqueACTH ELISA, Pituitary and Adrenal Cortical FunctionActivated Goalpha interacted directly with PLZF, and enhanced its function as a transcriptional and cell growth suppressor. Goalpha might play a role in mediating extracellular signal-regulated kinase Related articles to: The function of SCML1 remains unknown.
- BACKGROUND: Acute myocardial infarction (AMI) is a critical and fatal cardiovascular condition. The role of cuproptosis as an emerging mechanism in the pathogenesis of AMI remains to be fully elucidated. METHODS: Patient data were acquired from the Gene Expression Omnibus database. Differential expression analysis was performed on cuproptosis-related genes (CRGs). LASSO regression was employed to identify key CRGs and develop a diagnostic classification model for AMI. Weighted gene co-expression network analysis was performed to investigate key modules associated with the disease and its molecular classification. Subsequently, machine learning techniques were used to identify critical genes within these modules. The diagnostic efficacy of these genes for AMI was assessed using receiver operating characteristic analysis. The functions of the identified key genes were ultimately validated at the cellular level. RESULTS: Six characteristic CRGs were selected via LASSO regression. The AMI diagnostic classification model based on these CRGs demonstrated superior performance. Patients were classified into two subtypes related to cuproptosis, revealing significant differences in enrichment pathways between these subtypes. SYTL3, SCML1, and PMAIP1 were identified as key genes for AMI, with area under the curves of 0.813, 0.795, and 0.873, respectively. Knocking down PMAIP1 expression reduced intracellular copper levels in hypoxia-induced HUVECs. CONCLUSIONS: This study clarifies the role of cuproptosis in AMI and highlights the potential involvement of PMAIP1, providing a theoretical basis for further investigation into cuproptosis in AMI. - Source: PubMed
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