TTR
Anti-TTR Recombinant Antibody Products
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- Species Reactivity: Human
- Type: Human IgG
- Application: ELISA, DB, WB, IF
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- Species Reactivity: Human
- Type: Human scFv
- Application: ELISA, DB, WB, IF
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- Species Reactivity: Human
- Type: Human Fab
- Application: ELISA, DB, WB, IF
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- Species Reactivity: Human
- Type: Mouse IgG1, κ
- Application: ELISA, WB
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- Species Reactivity: Human
- Type: Mouse IgG1, κ
- Application: ELISA, WB
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- Derivation: Phage display library
- Species Reactivity: Human
- Type: Camel VHH
- Application: ELISA
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- Derivation: Phage display library
- Species Reactivity: Human
- Type: Camel VHH
- Application: ELISA
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- Species Reactivity: Human
- Type: Mouse scFv
- Application: ELISA, WB
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- Species Reactivity: Human
- Type: Mouse scFv
- Application: ELISA, WB
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- Species Reactivity: Human
- Type: Mouse Fab
- Application: ELISA, WB
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- Species Reactivity: Human
- Type: Mouse Fab
- Application: ELISA, WB
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- Species Reactivity: Human
- Type: Llama VHH
- Application: ELISA, Neut, ICC, FC
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- Species Reactivity: Human
- Type: Chicken antibody
- Application: Indirect ELISA, WB
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- Derivation: Phage display library
- Species Reactivity: Human
- Type: Rabbit IgG
- Application: FC, ICC, IHC-P, IP, WB
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For Research Use Only. Not For Clinical Use.
This gene encodes one of the three prealbumins, which include alpha-1-antitrypsin, transthyretin and orosomucoid. The encoded protein, transthyretin, is a homo-tetrameric carrier protein, which transports thyroid hormones in the plasma and cerebrospinal fluid. It is also involved in the transport of retinol (vitamin A) in the plasma by associating with retinol-binding protein. The protein may also be involved in other intracellular processes including proteolysis, nerve regeneration, autophagy and glucose homeostasis. Mutations in this gene are associated with amyloid deposition, predominantly affecting peripheral nerves or the heart, while a small percentage of the gene mutations are non-amyloidogenic. The mutations are implicated in the etiology of several diseases, including amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis and carpal tunnel syndrome.