Gauss

Hba1 mab (m02), clone 4f9 100 µg

Réf. UGAP : 3870969 Réf. Fournisseur : 16119184 Réf. Constructeur : H00003039-M02
Franco de port et d'emballage pour toutes les commandes supérieures à 80€ HT.

Produit ni repris ni échangé excepté en cas d’erreur du prestataire.
La quantité choisie doit être comprise entre 1 et 999 999.
Il ne reste que 0 exemplaires.

Points clés

Mouse monoclonal antibody raised against a partial recombinant HBA1.

The human alpha globin gene cluster located on chromosome 16 spans about 30kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported. [provided by RefSeq

En savoir plus

Garantie

Garantie 0 Mois

Description

Mouse monoclonal antibody raised against a partial recombinant HBA1.

The human alpha globin gene cluster located on chromosome 16 spans about 30kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported. [provided by RefSeq

Caractéristiques

Domaine de recherche
protéomique
Fournisseur
FISHER SCIENTIFIC S.A.S.
Marque
ABNOVA
Référence fabricant
H00003039-M02
Référence distributeur
16119184
Vendu par
100 ug
Quantité
N/A
Lieu de fabrication
Taiwan
Lieu de stockage
France
Délai de péremption à la date de livraison
12 mois
Code à barre
non
Soumis à carboglace
oui
Libellé produit fabricant
100ug hba1 monoclonal antibody (m02), clone 4f9
Certification
RUO
Marquage CE DIV
non
Type de produit
anticorps
Type de protéine
non
Type d'antibiotique
non
Type d'enzyme
non
Température de conservation (°C)
-192 °C
Température de transport
carboglace
Dispositif stérile
non
Type d'acide nucléique extrait
non
Origine humaine
non
Sans composant animal
non
Matière dangereuse
non
Autres caractéristiques
HBA1, Host Species: Mouse, Target Species: Human, Monoclonal, Western Blot, ELISA, Clone: 4F9, Primary, Unconjugated, 100 ug, Mouse monoclonal antibody raised against a partial recombinant HBA1., Liquid, PBS with no preservative; pH 7.4, NM_000558, H
Classification REACH
non
Code douanier
38229000
Nomenclature Nacres
NA.32
Nomenclature CEA
SGP01
Nomenclature IRSN
273
Nomenclature INSERM
NA.NA32
Nomenclature CNRS
NA32
Nomenclature CHU
18.551
Nomenclature DGOS
LD10AOOO
Type d’application
marquage
Type d'échantillon
protéine
Reprise en cas d’erreur client
non