SLC25A19 Antikörper
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- Target Alle SLC25A19 Antikörper anzeigen
- SLC25A19 (Solute Carrier Family 25 (Mitochondrial Thiamine Pyrophosphate Carrier), Member 19 (SLC25A19))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SLC25A19 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human SLC25A19 (NP_068380.3).
- Isotyp
- IgG
- Top Product
- Discover our top product SLC25A19 Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000 IF 1:50-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- SLC25A19 (Solute Carrier Family 25 (Mitochondrial Thiamine Pyrophosphate Carrier), Member 19 (SLC25A19))
- Andere Bezeichnung
- SLC25A19 (SLC25A19 Produkte)
- Synonyme
- zgc:111878 antikoerper, 2900089E13Rik antikoerper, DNC antikoerper, MUP1 antikoerper, TPC antikoerper, MCPHA antikoerper, THMD3 antikoerper, THMD4 antikoerper, solute carrier family 25 member 19 antikoerper, solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 antikoerper, Slc25a19 antikoerper, slc25a19 antikoerper, SLC25A19 antikoerper
- Hintergrund
- 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.
- Molekulargewicht
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Observed_MW: 36 kDa
Calculated_MW: 29 kDa/35 kDa
- Gen-ID
- 60386
- UniProt
- Q9HC21
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