PUS7L anticorps (AA 165-699)

N° du produit ABIN7871150

Cet anticorps Lapin Polyclonal détecte spécifiquement PUS7L dans WB, ELISA, IF et IHC (p). Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour PUS7L anticorps (AA 165-699) (ABIN7871150)

Antigène: PUS7L (Pseudouridylate Synthase 7 Homolog-Like (PUS7L))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PUS7L est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-PUS7L anticorps

Épitope: AA 165-699

Fonction: PUS7L Antibody / Pseudouridylate synthase 7 homolog-like protein

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (R165-H699) was used as the immunogen for the PUS7L antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the PUS7L antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the PUS7L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur PUS7L

Antigène: PUS7L (Pseudouridylate Synthase 7 Homolog-Like (PUS7L))

Autre désignation: PUS7L

Sujet: Pseudouridylate synthase 7 homolog-like protein is an enzyme that in humans is encoded by the PUS7L gene. PUS7L (pseudouridylate synthase 7 homolog (S. cerevisiae) -like) is a 701 amino acid protein that belongs to the pseudouridine synthase truD family and contains one TRUD domain. The PUS7L gene is conserved in chimpanzee, canine, bovine, mouse, chicken and zebrafish, and maps to human chromosome 12q12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.

UniProt: Q9H0K6