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GMA-067 datasheet
For in vitro research only. Not for use as a diagnostic or therapeutic. All sales governed by Warranty Policy located at: https://greenmoab. com/about-gma/warranty-policy/ Clone GM A-06 7 T h r o m b i n , i n t h e p r e s e n c e o f t h r […]
GMA-8014
[…] factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8014 (also known as 3G6 or 3G6.1B)1 recognizes the C2 domain of […]
GMA-8021
[…] factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+ . Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA- 8021 (also known as 2-76 or 76-1B) recognizes the A2 […]
GMA-8022
[…] factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8022 (also known as I14)1 recognizes the C2 domain of FVIII, is […]
GMA-8024
[…] factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+ . Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8024 (also known as 2-101) recognizes the A2 domain of FVIII […]
GMA-8025
[…] factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8025 (also known as 2D12) recognizes the C2 domain of FVIII […]
GMA-8026
[…] factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8026 (also known as G99)1 recognizes the C2 domain of FVIII through […]
GMA-8040
[…] Following activation by factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8040 is suitable for ELISA and Western blot applications.
GMA-8041
[…] Following activation by factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8041 is suitable for ELISA and Western blot applications.
GMA-8045
[…] von Willebrand factor. Following activation by factor Xa or thrombin, factor VIIIa can function as cofactor for the enzyme factor IXa in the activation of factor X in the presence of phospholipid and Ca2+. Absent or defective FVIII is the cause of the X-linked recessive bleeding disorder hemophilia A. GMA-8045 is suitable for ELISA applications.