Descrizione Azione

A synthesized peptide derived from human TRPS1, corresponding to a region within N-terminal amino acids.

Codice: DF3467 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human VR1, corresponding to a region within C-terminal amino acids.

Codice: DF10320 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human TRPV3, corresponding to a region within N-terminal amino acids.

Codice: DF10186 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human TRPV3, corresponding to a region within N-terminal amino acids.

Codice: BF8081 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human TRPV4, corresponding to a region within C-terminal amino acids.

Codice: DF8624 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human TRPV4, corresponding to a region within C-terminal amino acids.

Codice: BF9681 Confezionamento: 100ul
Dettagli

This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene.

Codice: E-AB-10664_20μL Confezionamento: 20μL
Dettagli

This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene.

Codice: E-AB-10664_60μL Confezionamento: 60μL
Dettagli

This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene.

Codice: E-AB-10664_120μL Confezionamento: 120μL
Dettagli

This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene.

Codice: E-AB-10664_200μL Confezionamento: 200μL
Dettagli

This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene.

Codice: E-AB-14424_120μL Confezionamento: 120μL
Dettagli

This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene.

Codice: E-AB-14424_60μL Confezionamento: 60μL
Dettagli