SLC25A19 antibody
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- Target See all SLC25A19 Antibodies
- SLC25A19 (Solute Carrier Family 25 (Mitochondrial Thiamine Pyrophosphate Carrier), Member 19 (SLC25A19))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This SLC25A19 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein of human SLC25A19 (NP_068380.3).
- Isotype
- IgG
- Top Product
- Discover our top product SLC25A19 Primary Antibody
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- Application Notes
- 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
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- 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))
- Alternative Name
- SLC25A19 (SLC25A19 Products)
- Synonyms
- zgc:111878 antibody, 2900089E13Rik antibody, DNC antibody, MUP1 antibody, TPC antibody, MCPHA antibody, THMD3 antibody, THMD4 antibody, solute carrier family 25 member 19 antibody, solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 antibody, Slc25a19 antibody, slc25a19 antibody, SLC25A19 antibody
- Background
- 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.
- Molecular Weight
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Observed_MW: 36 kDa
Calculated_MW: 29 kDa/35 kDa
- Gene ID
- 60386
- UniProt
- Q9HC21
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