C3orf39 anticorps (Biotin)
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- Antigène Voir toutes C3orf39 (GTDC2) Anticorps
- C3orf39 (GTDC2) (Glycosyltransferase-Like Domain Containing 2 (GTDC2))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C3orf39 est conjugé à/à la Biotin
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C3orf39
- Isotype
- IgG
- Top Product
- Discover our top product GTDC2 Anticorps primaire
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400 - Restrictions
- For Research Use only
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- 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 for 12 months.
- Date de péremption
- 12 months
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- 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
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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
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