GCM2 anticorps (AA 236-483)
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- Antigène Voir toutes GCM2 Anticorps
- GCM2 (Glial Cells Missing Homolog 2 (GCM2))
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Épitope
- AA 236-483
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp GCM2 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Purified by antigen-affinity chromatography.
- Immunogène
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 236 and 483 of human GCM2
- Top Product
- Discover our top product GCM2 Anticorps primaire
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- Indications d'application
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Suggested dilutions:
Western blotting: 1.500-1.3000 - Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
- Agent conservateur
- Thimerosal (Merthiolate)
- Précaution d'utilisation
- Biohazard Informations: This product contains thimerosal which is hazardous.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- Antigène
- GCM2 (Glial Cells Missing Homolog 2 (GCM2))
- Autre désignation
- glial cells missing homolog 2 (GCM2 Produits)
- Synonymes
- anticorps GCMb, anticorps Gcm-2, anticorps gcm-2, anticorps GCMB, anticorps hGCMb, anticorps Gcm-rs1, anticorps Gcm1, anticorps Gcm1-rs2, anticorps glial cells missing homolog 2, anticorps glial cells missing homolog 2 (Drosophila), anticorps glial cells missing homolog 2 S homeolog, anticorps GCM2, anticorps gcm2, anticorps gcm2.S, anticorps Gcm2
- Sujet
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This gene is a homolog of the Drosophila glial cells missing gene, which is thought to act as a binary switch between neuronal and glial cell determination.The protein encoded by this gene contains a conserved N-terminal GCM motif that has DNA-binding activity.The protein is a transcription factor that acts as a master regulator of parathyroid development.It has been suggested that this transcription factor might mediate the effect of calcium on parathyroid hormone expression and secretion in parathyroid cells.Mutations in this gene are associated with hypoparathyroidism.[provided by RefSeq]
- Poids moléculaire
- 57 kDa
- ID gène
- 9247
- NCBI Accession
- NM_004752, NP_004743
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