SLC25A4 抗体
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- 抗原 See all SLC25A4 抗体
- SLC25A4 (Solute Carrier Family 25 (Mitochondrial Carrier, Adenine Nucleotide Translocator), Member 4 (SLC25A4))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This SLC25A4 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human SLC25A4 (NP_001142.2).
- 亚型
- IgG
- Top Product
- Discover our top product SLC25A4 Primary Antibody
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- 应用备注
- WB 1:500-1:2000 IF 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- SLC25A4 (Solute Carrier Family 25 (Mitochondrial Carrier, Adenine Nucleotide Translocator), Member 4 (SLC25A4))
- 别名
- SLC25A4 (SLC25A4 产品)
- 别名
- 1 antibody, AAC1 antibody, ANT antibody, ANT 1 antibody, ANT1 antibody, PEO2 antibody, PEO3 antibody, T1 antibody, AU019225 antibody, Ant1 antibody, ant antibody, ant1 antibody, peo2 antibody, peo3 antibody, MANT1 antibody, SLC25A5 antibody, fa22e07 antibody, wu:fa22e07 antibody, zgc:77591 antibody, slc25a4 antibody, solute carrier family 25 member 4 antibody, solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 antibody, adenine nucleotide translocator antibody, solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 antibody, solute carrier family 25 member 4 L homeolog antibody, SLC25A4 antibody, Slc25a4 antibody, slc25a4 antibody, ANT1 antibody, slc25a4.L antibody
- 背景
- This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy.
- 分子量
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Observed_MW: 33 kDa
Calculated_MW: 33 kDa
- 基因ID
- 291
- UniProt
- P12235
- 途径
- Proton Transport, Dicarboxylic Acid Transport
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