Thermo Fisher Scientific Factor XIII Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA143050 | - | Thermo Fisher Scientific PA143050 Factor XIII Polyclonal Antibody 1 mg pk | 재고문의 | pk | 331,000원 | - | 364,100원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
25 µg/mL
ELISA (ELISA)
5-10 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Sheep / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Human Factor XIII.
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
9.8 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
Ambient (domestic); Wet ice (international)
RRID
AB_1074354
Product Specific Information
PA1-43050 detects Factor XIII in human samples.
PA1-43050 has successfully been used in Western blot and ELISA applications.
PA1-43050 was derived from human factor XIII.
Target Information
This gene encodes the coagulation factor XIII A subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. It also crosslinks alpha-2-plasmin inhibitor, or fibronectin, to the alpha chains of fibrin. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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