PIK3IP1 Protein (His tag)

N° du produit ABIN7318904

Détail du produit

Antigène: PIK3IP1 (Phosphoinositide-3-Kinase-Interacting Protein 1 (PIK3IP1))

Type de proteíne: Recombinant

Origine: Humain

Source: Human Cells

Purification/Conjugué: Cette PIK3IP1 protéine est marqué à la His tag.

Fonction: Recombinant Human PIK3IP1 Protein (His Tag)

Séquence: Ser22-Thr168

Attributs du produit: Recombinant Human Phosphoinositide-3-kinase-interacting protein 1 is produced by our Mammalian expression system and the target gene encoding Ser22-Thr168 is expressed with a 6His tag at the C-terminus.

Pureté: > 95 % as determined by reducing SDS-PAGE.

niveau d'endotoxine: < 1.0 EU per μg as determined by the LAL method.

Information d'application

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Please refer to the printed manual for detailed information.

Buffer: Lyophilized from a 0.2 μm filtered solution of 50 mM TrisHCl,10 mM reduced Glutathione,PH8.0.

Stock: 4 °C,-20 °C,-80 °C

Stockage commentaire: Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.

Détail du antigène

Antigène: PIK3IP1 (Phosphoinositide-3-Kinase-Interacting Protein 1 (PIK3IP1))

Autre désignation: PIK3IP1 (PIK3IP1 Produits)

Synonymes: HGFL Protein, hHGFL(S) Protein, 1500004A08Rik Protein, 5830455E04Rik Protein, Crkd Protein, Hgfl Protein, RGD1311203 Protein, zgc:66482 Protein, phosphoinositide-3-kinase interacting protein 1 Protein, PIK3IP1 Protein, Pik3ip1 Protein

Sujet:

Background: Phosphoinositide-3-kinase-interacting protein 1(PIK3IP1) is an enzyme that in humans is encoded by the PIK3IP1 gene.It is a negative regulator of phosphatidylinositol-3-kinase (PI3K), suppresses the development of hepatocellular carcinoma. The gene encoding PIK3IP1 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.

Synonym: Kringle domain-containing protein HGFL, PIK3IP1, HGFL

Poids moléculaire: 16.7 kDa

UniProt: Q96FE7