Factor VIII antibody (AA 2130-2210)
Quick Overview for Factor VIII antibody (AA 2130-2210) (ABIN7214840)
Target
See all Factor VIII (F8) AntibodiesReactivity
Host
Clonality
Conjugate
Application
-
-
Binding Specificity
- AA 2130-2210
-
Purpose
- Factor VIII Polyclonal Antibody
-
Specificity
- Factor VIII Polyclonal Antibody detects endogenous levels of Factor VIII protein.
-
Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
-
Immunogen
- Synthesized peptide derived from the C-terminal region of human Factor VIII at AA range: 2130-2210
-
Isotype
- IgG
-
-
-
-
Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:10000). Not yet tested in other applications.
-
Comment
-
Primary Antibody
-
Restrictions
- For Research Use only
-
-
-
Format
- Liquid
-
Concentration
- 1 mg/mL
-
Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
-
Preservative
- Sodium azide
-
Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Storage
- -20 °C
-
Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
-
-
- Factor VIII (F8) (Coagulation Factor VIII (F8))
-
Alternative Name
- Factor VIII
-
Background
- Rabbit Anti-Factor VIII Polyclonal Antibody,F8, F8C, Coagulation factor VIII, Antihemophilic factor, AHF, Procoagulant component,F8 encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation, factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. F8 produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. DefectsF8 results in hemophilia A, a common recessive X-linked coagulation disorder.,Coagulation factor VIII
-
Molecular Weight
- observerd band 300kDa
-
Gene ID
- 2157
-
UniProt
- P00451
Target
-