Coagulation Factor IX Protein (F9) (AA 1-471) (His tag)
Quick Overview for Coagulation Factor IX Protein (F9) (AA 1-471) (His tag) (ABIN7505722)
Target
See all Coagulation Factor IX (F9) ProteinsProtein Type
Origin
Source
Purity
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Protein Characteristics
- AA 1-471
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Purification tag / Conjugate
- This Coagulation Factor IX protein is labelled with His tag.
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Sequence
- Met 1-Thr 471
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Characteristics
- A DNA sequence encoding the full length of mouse F9 (P16294) (Met 1-Thr 471) was fused with a polyhistidine tag at the C-terminus and a signal peptide at the N-terminus.
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Endotoxin Level
- <1.0 EU per μg of the protein as determined by the LAL method.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Buffer
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Lyophilized from sterile PBS, pH 7.4.
Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween80 are added as protectants before lyophilization. -
Storage
- 4 °C,-20 °C,-80 °C
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Storage Comment
- Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
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Expiry Date
- 12 months
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- Coagulation Factor IX (F9)
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Alternative Name
- Coagulation Factor IX
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Background
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Abbreviation: Coagulation Factor IX,F9
Target Synonym: AW111646,Cf-9,Cf9
Background: Coagulation factor IX, also known as Christmas factor, Plasma thromboplastin component and PTC, is a secreted protein which belongs to the peptidase S1 family. Coagulation factor IX / F9 contains two EGF-like domains, one Gla (gamma-carboxy-glutamate) domain and one?peptidase S1 domain. Coagulation factor IX / F9 is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca2+ons, phospholipids, and factor VIIIa. Defects in Coagulation factor IX / F9 are the cause of thrombophilia due to factor IX defect which is a hemostatic disorder characterized by a tendency to thrombosis. Defects in Coagulation factor IX / F9 are also the cause of recessive X-linked hemophilia B ( HEMB ) which also known as Christmas disease.
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Molecular Weight
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Calculated MW: 51.3 kDa
Observed MW: 60-80 kDa
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UniProt
- P16294
Target
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