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- Target See all COL3 Proteins
- COL3 (Collagen, Type III (COL3))
- Protein Type
- Native
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Origin
- Human
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Source
- Human
- Characteristics
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Purified native Human Collagen Type III protein
Protein Source: Human placenta - Purification
- Affinity chromatography
- Sterility
- Sterile filtered
- Top Product
- Discover our top product COL3 Protein
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Collagen, Type III (COL3) protein
COL3 Origin: Human Host: Human Native ELISA, IHC, WB
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Sterile filtered liquid in 0.5 M CH3COOH, with 0.01 % NaN3.
- Preservative
- Sodium azide
- Precaution of Use
- WARNING: Reagents contain sodium azide. Sodium azide is very toxic if ingested or inhaled. Avoid contact with skin, eyes, or clothing. Wear eye or face protection when handling. If skin or eye contact occurs, wash with copious amounts of water. If ingested or inhaled, contact a physician immediately. Sodium azide yields toxic hydrazoic acid under acidic conditions. Dilute azide-containing compounds in running water before discarding to avoid accumulation of potentially explosive deposits in lead or copper plumbing.
- Handling Advice
- Dilute only prior to immediate use.
- Storage
- 4 °C
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- Target
- COL3 (Collagen, Type III (COL3))
- Alternative Name
- Collagen Type III (COL3 Products)
- Synonyms
- PT Protein, RPRGL2 Protein, THPH1 Protein, Cf-2 Protein, Cf2 Protein, FII Protein, thrombin Protein, prothrombin Protein, coagulation factor II, thrombin Protein, coagulation factor II Protein, F2 Protein
- Background
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Collagen III is a fibrillar collagen that is found in extensible connective tissues such as skin, lung, and the vascular system, frequently in association with type I Collagen. Mutations in the gene are associated with Ehlers Danlos syndrome type IV, and with aortic and arterial aneurysms. Although alternate transcripts have been detected for this gene, they are the result of mutations, these mutations alter splicing, often leading to the exclusion of multiple exons. .
Description: Human placenta.
Alternative Names: Fetal collagen protein, Collagen type III alpha 1 protein, Ehlers Danlos syndrome type IV, Collagen type III alpha protein, autosomal dominant protein, EDS4A protein
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