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Thermo Fisher Scientific Human Factor X Native Protein
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Thermo Fisher Scientific Human Factor X Native Protein

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인체 혈장 유래의 Native Factor X 단백질로, 면역학적 분석의 양성 대조군으로 사용 가능. 6.5 mg/mL 농도의 액상 형태이며, SDS-PAGE로 정제됨. -20°C에서 보관하며, 연구용으로만 사용 가능.

카탈로그번호
RP43072
카테고리
Protein
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 09:20
Thermo Fisher Scientific RP43072 Human Factor X Native Protein 100 ug pk판매 단위 pk
재고 1개
263,000원VAT 포함 289,300원

Thermo Fisher Scientific · Thermo Fisher Scientific Human Factor X Native Protein

Applications

  • Control (Ctrl): Assay-dependent

Product Specifications

항목 내용
Species Human
Molecular Weight 58.9 kDa
Class Native
Type Protein
Conjugate Unconjugated
Form Liquid
Concentration 6.5 mg/mL
Purification SDS-PAGE
Storage Buffer 50% water with 50% glycerol
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice

Product Specific Information

RP-43072 contains native human Factor X protein purified from blood/plasma.
This product may be used as a positive control in various immunological assays.
The product is derived from human blood/plasma. Although the starting material was tested and found negative or nonreactive for anti-HIV-1/2, HIV-1 antigens, HBsAg, STS, anti-HCV, anti-HBcore, and anti-HTLV I & II, extreme caution should be exercised when handling this material due to the inherent margin of error in all tests.
For in vitro research use only. Not intended for clinical or diagnostic use.

Target Information

F10 undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by excision of the tripeptide RKR.
Two chains of the factor are linked by one or more disulfide bonds:

  • The light chain contains two EGF-like domains.
  • The heavy chain contains the catalytic domain, structurally homologous to other hemostatic serine proteases.

The mature factor is activated by cleavage of the activation peptide by factor IXa (intrinsic pathway) or by factor VIIa (extrinsic pathway).
Activated Factor X converts prothrombin to thrombin in the presence of factor Va, Ca²⁺, and phospholipid during blood clotting.
Mutations in this gene cause factor X deficiency, a hemorrhagic disorder of variable severity.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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