SLC25A12 antibody
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- Target See all SLC25A12 (Slc25a12) Antibodies
- SLC25A12 (Slc25a12) (Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12))
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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 SLC25A12 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein of human SLC25A12 (NP_003696.2).
- Isotype
- IgG
- Top Product
- Discover our top product Slc25a12 Primary Antibody
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- Application Notes
- 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
- 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
- SLC25A12 (Slc25a12) (Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12))
- Alternative Name
- SLC25A12 (Slc25a12 Products)
- Synonyms
- cb929 antibody, cb1094 antibody, zgc:66248 antibody, wu:fj94c07 antibody, AGC1 antibody, ARALAR antibody, Aralar1 antibody, RGD1561141 antibody, ARALAR1 antibody, 2610002D09Rik antibody, AI839531 antibody, B230107K20Rik antibody, BB129864 antibody, solute carrier family 25 (aspartate/glutamate carrier), member 12 antibody, solute carrier family 25 member 12 antibody, solute carrier family 25 member 12 L homeolog antibody, solute carrier family 25 (mitochondrial carrier, Aralar), member 12 antibody, slc25a12 antibody, SLC25A12 antibody, slc25a12.L antibody, Slc25a12 antibody
- Background
- 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.
- Molecular Weight
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Observed_MW: 75 kDa
Calculated_MW: 62 kDa/74 kDa
- Gene ID
- 8604
- UniProt
- O75746
- Pathways
- Ribonucleoside Biosynthetic Process, Dicarboxylic Acid Transport
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