SLC25A19 anticorps
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- Antigène Voir toutes SLC25A19 Anticorps
- SLC25A19 (Solute Carrier Family 25 (Mitochondrial Thiamine Pyrophosphate Carrier), Member 19 (SLC25A19))
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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 SLC25A19 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein of human SLC25A19 (NP_068380.3).
- Isotype
- IgG
- Top Product
- Discover our top product SLC25A19 Anticorps primaire
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- Indications d'application
- WB 1:500-1:2000 IF 1:50-1:200
- 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
- SLC25A19 (Solute Carrier Family 25 (Mitochondrial Thiamine Pyrophosphate Carrier), Member 19 (SLC25A19))
- Autre désignation
- SLC25A19 (SLC25A19 Produits)
- Synonymes
- anticorps zgc:111878, anticorps 2900089E13Rik, anticorps DNC, anticorps MUP1, anticorps TPC, anticorps MCPHA, anticorps THMD3, anticorps THMD4, anticorps solute carrier family 25 member 19, anticorps solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19, anticorps Slc25a19, anticorps slc25a19, anticorps SLC25A19
- Sujet
- This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria, further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier, which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly, Amish type, a metabolic disease that results in severe congenital microcephaly, severe 2-ketoglutaric aciduria, and death within the first year. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene.
- Poids moléculaire
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Observed_MW: 36 kDa
Calculated_MW: 29 kDa/35 kDa
- ID gène
- 60386
- UniProt
- Q9HC21
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