Tpm1 (human) recombinant (full leng ht protein gst tag) 10 µg
Produit ni repris ni échangé excepté en cas d’erreur du prestataire.
Points clés
Used for AP, Array, ELISA, WB-Re
This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy. [provided by RefSeq]
Garantie
Garantie 0 Mois
Description
Used for AP, Array, ELISA, WB-Re
This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy. [provided by RefSeq]
Caractéristiques
- Type d'antibiotique
- non
- Marque
- ABNOVA
- Référence distributeur
- 16123778
- Fournisseur
- FISHER SCIENTIFIC S.A.S.
- Dispositif stérile
- non
- Marquage CE DIV
- non
- Code à barre
- non
- Type d'acide nucléique extrait
- non
- Origine humaine
- non
- Sans composant animal
- non
- Vendu par
- 10 ug
- Délai de péremption à la date de livraison
- 12 mois
- Température de conservation (°C)
- -80 °C
- Température de transport
- carboglace
- Soumis à carboglace
- oui
- Classification REACH
- non
- Code douanier
- 38229000
- Nomenclature IFPEN
- NA.55
- Nomenclature DGOS
- LD10AOOO
- Domaine de recherche
- protéomique
- Reprise en cas d’erreur client
- non
- Libellé produit fabricant
- 10ug tpm1 (human) recombinant protein (p01)
- Nomenclature Nacres
- NA.55
- Type de produit
- protéine
- Nomenclature IRSN
- 273
- Nomenclature INSERM
- NA.NA55
- Type d’application
- ELISA, western blot
- Lieu de stockage
- France
- Nomenclature CHU
- 18.551
- Autres caractéristiques
- Abnova Human TPM1 Full-length ORF (NP_001018008.1, 1 a.a. - 245 a.a.) Recombinant Protein with GST-tag at N-terminal, Quantity: 10 ug, Format: Liquid, Formulation: 50mM Tris-HCI, 10mM reduced Glutathione, pH-8.0 in the elution buffer., Host Species:
- Lieu de fabrication
- Taïwan
- Nomenclature CEA
- SGP01
- Nomenclature CNRS
- NA55
- Matière dangereuse
- non
- Type d'échantillon
- protéine
- Quantité
- N/A
- Type d'enzyme
- non
- Type de protéine
- oui
- Référence fabricant
- H00007168-P01
- Certification
- RUO

