
Thermo Fisher Scientific Factor VIII Recombinant Rabbit Monoclonal Antibody (610)
인체 응고인자 VIII(F8)을 특이적으로 인식하는 Thermo Fisher의 재조합 토끼 단일클론 항체. ELISA에 적합하며 높은 특이성과 일관성을 제공. 보존제가 없는 PBS 용액 형태로 제공되며 장기 보관 시 -20°C에서 보관 권장.
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Applications
- ELISA (ELISA)
Tested Dilution: 1:5,000–1:10,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host/Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | 610 |
| Immunogen | Recombinant Human Coagulation Factor VIII/FVIII/F8 Protein |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage buffer | PBS |
| Contains | No preservative |
| Storage conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2786294 |
Product Specific Information
This product is preservative-free. It is recommended to add sodium azide to avoid contamination (final concentration 0.05%–0.1%).
Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. These systems are developed by cloning specific antibody DNA sequences from immunoreactive rabbits. Individual clones are screened to select optimal candidates for production.
Advantages of recombinant rabbit monoclonal antibodies:
- Better specificity and sensitivity
- Lot-to-lot consistency
- Animal origin-free formulations
- Broader immunoreactivity due to larger rabbit immune repertoire
This antibody has specificity for Human Coagulation Factor VIII/FVIII/F8.
Target Information
The gene encodes coagulation factor VIII, a cofactor in the intrinsic pathway of blood coagulation. Factor VIII acts with factor IXa, Ca²⁺, and phospholipids to convert factor X to its activated form Xa.
Two alternatively spliced transcripts are produced:
- Transcript variant 1 (isoform a): Large glycoprotein circulating in plasma, forms a noncovalent complex with von Willebrand factor.
- Transcript variant 2 (isoform b): Small protein primarily consisting of the phospholipid-binding domain essential for coagulant activity.
Defects in this gene result in Hemophilia A, a common recessive X-linked coagulation disorder.
For Research Use Only.
Not for use in diagnostic procedures. Not for resale without express authorization.
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