SLC25A12 anticorps
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- Antigène Voir toutes SLC25A12 (Slc25a12) Anticorps
- SLC25A12 (Slc25a12) (Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12))
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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 SLC25A12 est non-conjugé
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Application
- Western Blotting (WB)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein of human SLC25A12 (NP_003696.2).
- Isotype
- IgG
- Top Product
- Discover our top product Slc25a12 Anticorps primaire
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- Indications d'application
- WB 1:500-1:2000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- 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 -20°C. Avoid freeze / thaw cycles.
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- Antigène
- SLC25A12 (Slc25a12) (Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12))
- Autre désignation
- SLC25A12 (Slc25a12 Produits)
- Synonymes
- anticorps cb929, anticorps cb1094, anticorps zgc:66248, anticorps wu:fj94c07, anticorps AGC1, anticorps ARALAR, anticorps Aralar1, anticorps RGD1561141, anticorps ARALAR1, anticorps 2610002D09Rik, anticorps AI839531, anticorps B230107K20Rik, anticorps BB129864, anticorps solute carrier family 25 (aspartate/glutamate carrier), member 12, anticorps solute carrier family 25 member 12, anticorps solute carrier family 25 member 12 L homeolog, anticorps solute carrier family 25 (mitochondrial carrier, Aralar), member 12, anticorps slc25a12, anticorps SLC25A12, anticorps slc25a12.L, anticorps Slc25a12
- Sujet
- This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene.
- Poids moléculaire
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Observed_MW: 75 kDa
Calculated_MW: 62 kDa/74 kDa
- ID gène
- 8604
- UniProt
- O75746
- Pathways
- Ribonucleoside Biosynthetic Process, Dicarboxylic Acid Transport
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