
Thermo Fisher Scientific Factor VIII Recombinant Rabbit Monoclonal Antibody (226)
인체 Coagulation Factor VIII에 특이적인 재조합 토끼 단클론 항체로 높은 특이성과 민감도를 제공. ELISA에 적합하며 로트 간 일관성 및 동물 유래 성분이 없는 포뮬레이션. 단기 4°C, 장기 -20°C 보관 권장.
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- MA530579
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- pk
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Applications
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 | 226 |
| 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_2786292 |
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. The expression systems are developed by cloning the specific antibody DNA sequences from immunoreactive rabbits. Individual clones are screened to select the best candidates for production.
Advantages of recombinant rabbit monoclonal antibodies:
- Better specificity and sensitivity
- Lot-to-lot consistency
- Animal origin-free formulations
- Broader immunoreactivity to diverse targets due to larger rabbit immune repertoire
This antibody has specificity for Human Coagulation Factor VIII/FVIII/F8 Heavy Chain.
Target Information
This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation. Factor VIII acts as a cofactor for factor IXa, which, in the presence of Ca²⁺ and phospholipids, converts factor X to the activated form Xa.
Two alternatively spliced transcripts are produced:
- Transcript variant 1: Encodes a large glycoprotein (isoform a) that circulates in plasma and associates with von Willebrand factor in a noncovalent complex.
- Transcript variant 2: Encodes a smaller protein (isoform b) consisting primarily 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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