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Thermo Fisher Scientific Factor VIII Recombinant Rabbit Monoclonal Antibody (226)
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Thermo Fisher Scientific Factor VIII Recombinant Rabbit Monoclonal Antibody (226)

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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.

카탈로그번호
MA530579
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 02:58
Thermo Fisher Scientific MA530579 Factor VIII Recombinant Rabbit Monoclonal Antibody (226) 100 ul pk판매 단위 pk ·
재고 확인 필요
569,900원VAT 포함 626,890원

Thermo Fisher Scientific · Thermo Fisher Scientific Factor VIII Recombinant Rabbit Monoclonal Antibody (226)

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:

  1. Transcript variant 1: Encodes a large glycoprotein (isoform a) that circulates in plasma and associates with von Willebrand factor in a noncovalent complex.
  2. 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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