C3orf39 anticorps (Alexa Fluor 680)

N° du produit ABIN4998459

Détail du produit anti-C3orf39 anticorps (Alexa Fluor 680)

Antigène: C3orf39 (GTDC2) (Glycosyltransferase-Like Domain Containing 2 (GTDC2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C3orf39 est conjugé à/à la Alexa Fluor 680

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C3orf39

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur C3orf39

Antigène: C3orf39 (GTDC2) (Glycosyltransferase-Like Domain Containing 2 (GTDC2))

Autre désignation: C3orf39 (GTDC2 Produits)

Synonymes: anticorps AGO61, anticorps C3orf39, anticorps GTDC2, anticorps C22H3orf39, anticorps C23H3orf39, anticorps ago61, anticorps Ago61, anticorps C85492, anticorps RGD1304827, anticorps MDDGA8, anticorps protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-), anticorps protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2, anticorps POMGNT2, anticorps Pomgnt2

Sujet:

Synonyms: AGO61, Chromosome 3 open reading frame 39, FLJ14566, Uncharacterized glycosyltransferase AGO61 precursor, GTDC2_HUMAN.

Background: C3orf39, also known as AGO61, is a 580 amino acid secreted protein belonging to the glycosyltransferase 61 family. C3orf39 is encoded by a gene that maps to human chromosome 3p25.1. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.

ID gène: 84892