DGCR14 anticorps
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- Antigène Voir toutes DGCR14 Anticorps
- DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))
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Reactivité
- Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp DGCR14 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogène
- Recombinant Protein of human DGCR14
- Isotype
- IgG
- Top Product
- Discover our top product DGCR14 Anticorps primaire
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- Indications d'application
- WB 1:500 - 1:2000
- Commentaires
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Highly expressed in heart, brain and skeletal muscle, Detected at low levels in placenta
- Restrictions
- For Research Use only
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- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20C. Avoid freeze / thaw cycles.
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- Antigène
- DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))
- Autre désignation
- DGCR14 (DGCR14 Produits)
- Synonymes
- anticorps DGCR13, anticorps DGS-H, anticorps DGS-I, anticorps DGSH, anticorps DGSI, anticorps ES2, anticorps Es2el, anticorps AI462402, anticorps D16H22S1269E, anticorps Dgcr1, anticorps Dgsi, anticorps fc19d10, anticorps wu:fc19d10, anticorps zgc:162979, anticorps MGC82189, anticorps DGCR14, anticorps es2, anticorps dgsi, anticorps dgs-h, anticorps dgs-i, anticorps es2el, anticorps dgcr13, anticorps ess-2 splicing factor homolog, anticorps DiGeorge syndrome critical region gene 14, anticorps ess-2 splicing factor homolog S homeolog, anticorps ESS2, anticorps Dgcr14, anticorps ess2, anticorps Ess2, anticorps DGCR14, anticorps ess2.S
- Sujet
- This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. Alternatively spliced transcript variants have been found for this gene.
- Poids moléculaire
- 52.568 kDa
- ID gène
- 8220
- UniProt
- Q96DF8
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