pCBRG-RUNX2 RE
CBV20086
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| Introduction | |
| Description: | pRUNX2 RE-Luc is designed for monitoring the induction of runt-related transcription factor 1. RUNX2 (RUNX Family Transcription Factor 2) is a Protein Coding gene. Diseases associated with RUNX2 include Cleidocranial Dysplasia and Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly. Among its related pathways are Notch Signaling Pathway (WikiPathways) and Gene Expression. Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity and RNA polymerase II proximal promoter sequence-specific DNA binding. |
| Plasmid profile: |  |
| Unit Size: | 1-4μg |
| Pathway (Activitor): | RUNT-RELATED?TRANSCRIPTION?FACTOR |
| Pathway profile: |  |
| Full Name: | RUNT-RELATED?TRANSCRIPTION?FACTOR 2 |
| Cis response element: | RUNX2 RE |
| Shelf Life: | One year from date of receipt under proper storage conditions. |
| Storage: | -20°C |
| Mode of transportation: | Ice bag transport |
| Matters needing attention: | For your health, please wear lab clothes and disposable gloves. |
