Thermo Fisher Scientific GTF2I Monoclonal Antibody (3F4)
GTF2I 단백질을 표적으로 하는 Thermo Fisher Scientific의 단일클론 항체(3F4). 인간에 반응하며 ELISA에서 10 µg/mL로 검증됨. 액상 형태, 보존제 없음, -20°C에서 보관. 연구용으로만 사용 가능.
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Applications
- ELISA (ELISA)
Tested Dilution: 10 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgM, kappa |
| Class | Monoclonal |
| Type | Antibody |
| Clone | 3F4 |
| Immunogen | GTF2I (AAH04472, 1 a.a. ~ 274 a.a) full-length recombinant protein with GST tag (MW of GST tag alone: 26 KDa) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | See Label |
| Storage Buffer | Ascites |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
Sequence of this protein is as follows:
MAQVAMSTLP VEDEESSESR MVVTFLMSAL ESMCKELAKS KAEVACIAVY ETDVFVVGTE RGRAFVNTRK DFQKDFVKYC VEEEEKAAEM HKMKSTTQAN RMSVDAVEIE TLRKTVEDYF CFCYGKALGK STVVPVPYEK MLRDQSAVVV QGLPEGVAFK HPENYDLATL KWILENKAGV SFIIKRPFLE PKKHVGGRVM VTDADRSILS PGGSCGPIKV KTEPTEDSGI SLEMAAVTVK EESEDPDYYQ YNIQGSHHSS EGNEGTEMEV PAEG
Target Information
This gene encodes a multifunctional phosphoprotein involved in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.
Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13, and 21.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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