RPUSD2 anticorps

N° du produit ABIN1387113

Détail du produit anti-RPUSD2 anticorps

Antigène: RPUSD2 (RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RPUSD2 est non-conjugé

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human RPUSD2

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur RPUSD2

Antigène: RPUSD2 (RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2))

Autre désignation: RPUSD2 (RPUSD2 Produits)

Synonymes: anticorps RPUSD2, anticorps C15orf19, anticorps C18B11, anticorps 4921503C21Rik, anticorps 9630001E10, anticorps BB231107, anticorps RGD1306147, anticorps RNA pseudouridylate synthase domain containing 2, anticorps RPUSD2, anticorps Rpusd2

Sujet:

Synonyms: C15orf19, C18B11, C18B11 homolog, RNA pseudouridylate synthase domain containing 2, RNA pseudouridylate synthase domain containing protein 2, RNA pseudouridylate synthase domain-containing protein 2, RPUSD 2, RPUSD-2, RUSD2_HUMAN.

Background: RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

ID gène: 27079