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Thermo Fisher Scientific F13A1 Monoclonal Antibody (OTI6F5), TrueMAB
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Thermo Fisher Scientific F13A1 Monoclonal Antibody (OTI6F5), TrueMAB

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인간 F13A1 단백질을 인식하는 마우스 단클론 항체로 ELISA 및 Luminex 분석에 적합. 고순도 친화 크로마토그래피 정제 제품. PBS 완충액에 보존되어 안정적이며, 연구용으로만 사용 가능.

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pk
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마지막 업데이트 2025. 08. 05. 오전 10:23
Thermo Fisher Scientific TA600091 F13A1 Monoclonal Antibody (OTI6F5), TrueMAB 100 ug pk판매 단위 pk ·
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615,900원VAT 포함 677,490원

Thermo Fisher Scientific · Thermo Fisher Scientific F13A1 Monoclonal Antibody (OTI6F5), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
ELISA (ELISA) 1:100–1:1,000
Luminex (LUM) 1:100–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI6F5
Immunogen Full length human recombinant protein of human F13A1 produced in HEK293T cells
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with <5% trehalose
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice

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 two A subunits and two B subunits. The A subunits have catalytic function, while the B subunits serve as plasma carrier molecules. Platelet factor XIII consists only of two A subunits identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ions, plasma factor XIII dissociates its B subunits and yields the active enzyme, factor XIIIa, identical to platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinks between fibrin molecules, 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 (lack of both A and B subunits) and type II deficiency (lack of A subunit alone). These defects can result in 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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