
Thermo Fisher Scientific TMPRSS12 Polyclonal Antibody
TMPRSS12 단백질을 인식하는 토끼 폴리클로날 항체로, Western blot에 최적화되어 있습니다. 인간 시료에 반응하며, 합성 펩타이드로부터 제작되었습니다. 액상 형태로 제공되며, -20°C에서 보관합니다. 연구용으로만 사용 가능합니다.
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Applications
Western Blot (WB)
- Tested Dilution: 0.2–1.0 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide directed towards the middle region of human TMPRSS12 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS with 2% sucrose |
| Contains | 0.09% sodium azide |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Wet ice |
| RRID | AB_2689063 |
Product Specific Information
This target displays homology in the following species:
- Guinea Pig: 86%
- Human: 100%
- Rabbit: 79%
- Rat: 86%
Target Information
TMPRSS12 (transmembrane protease serine 12) is a 348 amino acid single-pass membrane protein belonging to the peptidase S1 family and contains one peptidase S1 domain. The TMPRSS12 gene consists of approximately 45,000 bases and maps to human chromosome 12q13.12. Chromosome 12 encodes over 1,100 genes within 132 million bases, representing about 4.5% of the human genome. Several skeletal deformities, including hypochondrogenesis, achondrogenesis, and Kniest dysplasia, are linked to chromosome 12. Noonan syndrome, associated with cardiac and facial developmental defects, results from mutations in the PTPN11 gene (SH-PTP2). Chromosome 12 also contains a homeobox gene cluster essential for morphogenesis and a natural killer complex gene cluster encoding C-type lectin proteins involved in NK cell responses to MHC I interaction. Trisomy 12p is associated with facial developmental defects, seizure disorders, and variable severity depending on mosaicism extent.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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