AGXT 抗体
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- 抗原 See all AGXT 抗体
- AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
- 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 AGXT antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA
- 纯化方法
- Affinity purification
- 免疫原
- Synthetic peptide of human AGXT
- 亚型
- IgG
- Top Product
- Discover our top product AGXT Primary Antibody
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anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 96-125) antibody
AGXT 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB18848 unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 120-334) antibodyAGXT 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 112-294) antibodyAGXT 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 182-371) antibodyAGXT 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) antibodyAGXT 适用: 人, 小鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (Internal Region) antibodyVerified AGXT 适用: 人 ELISA, FACS, IF 宿主: 山羊 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 187-741) antibodyAGXT 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 183-392) antibodyAGXT 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) (AA 188-375) antibodyAGXT 适用: 人 WB 宿主: 小鼠 Monoclonal 1739CT804-82-83-1 unconjugated
anti-Alanine Glyoxylate Aminotransferase (AGXT) antibodyAGXT 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
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- 浓度
- 0.6 mg/mL
- 缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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
- AGXT (Alanine Glyoxylate Aminotransferase (AGXT))
- 别名
- AGXT (AGXT 产品)
- 别名
- AGT antibody, AGT1 antibody, AGXT1 antibody, PH1 antibody, SPAT antibody, SPT antibody, TLH6 antibody, Spat antibody, Agt1 antibody, Agxt1 antibody, agt antibody, agt1 antibody, agxt antibody, agxt1 antibody, spt antibody, agxtl antibody, zgc:91879 antibody, wu:fb57d01 antibody, zgc:65930 antibody, alanine-glyoxylate aminotransferase antibody, serine--pyruvate aminotransferase, mitochondrial antibody, alanine-glyoxylate aminotransferase L homeolog antibody, alanine-glyoxylate aminotransferase a antibody, alanine-glyoxylate aminotransferase b antibody, AGXT antibody, Agxt antibody, LOC607355 antibody, agxt.L antibody, agxta antibody, agxtb antibody
- 背景
- AGT,AGT1,Agxt,AGXT1,Alanine glyoxylate aminotransferase,Alanine glyoxylate aminotransferase3,Alanine--glyoxylate aminotransferase,EC 2.6.1.44,EC 2.6.1.51,Hepatic peroxisomal alanine glyoxylate aminotransferase,Hepatic peroxisomal alanine:glyoxylate aminotransferase,L alanine glyoxylate aminotransferase 1,MS773,PH1,Serine pyruvate aminotransferase,Serine--pyruvate aminotransferase,Serine--pyruvate aminotransferase,mitochondrial,Serine:pyruvate aminotransferase,SPAT,SPT,SPYA,TLH6,Serine-pyruvate aminotransferase is an enzyme that in humans is encoded by the AGXT gene. This gene is expressed only in the liver and the encoded protein is localized mostly in the peroxisomes, where it is involved in glyoxylate detoxification. Mutations in this gene, some of which alter subcellular targetting, have been associated with type I primary hyperoxaluria. Defects in AGXT are the cause of hyperoxaluria primary type 1 (HP1), also known as primary hyperoxaluria type I (PH1) and oxalosis I. HP1 is a rare autosomal recessive inborn error of glyoxylate metabolism characterized by increased excretion of oxalate and glycolate, and the progressive accumulation of insoluble calcium oxalate in the kidney and urinary tract.
- 分子量
- 43 kDa
- NCBI登录号
- NP_000021
- UniProt
- P21549
- 途径
- Monocarboxylic Acid Catabolic Process, Dicarboxylic Acid Transport
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