SLC22A5 抗体 (AA 1-180)
Quick Overview for SLC22A5 抗体 (AA 1-180) (ABIN3022379)
抗原
See all SLC22A5 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1-180
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序列
- MRDYDEVTAF LGEWGPFQRL IFFLLSASII PNGFTGLSSV FLIATPEHRC RVPDAANLSS AWRNHTVPLR LRDGREVPHS CRRYRLATIA NFSALGLEPG RDVDLGQLEQ ESCLDGWEFS QDVYLSTIVT EWNLVCEDDW KAPLTISLFF VGVLLGSFIS GQLSDRFGRK NVLFVTMGMQ
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Polyclonal Antibodies
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human SLC22A5 (NP_003051.1).
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亚型
- IgG
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anti-Solute Carrier Family 22 Member 5 (SLC22A5) (AA 42-142) antibody
SLC22A5 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 22 Member 5 (SLC22A5) antibodySLC22A5 适用: 人, 大鼠, 小鼠 IHC 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 22 Member 5 (SLC22A5) (C-Term) antibodySLC22A5 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 22 Member 5 (SLC22A5) antibodySLC22A5 适用: 人, 大鼠, 小鼠 IF 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 22 Member 5 (SLC22A5) (C-Term) antibodySLC22A5 适用: 人, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 22 Member 5 (SLC22A5) (AA 305-354) antibodySLC22A5 适用: 人, 大鼠, Cow, 马, 犬, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid freeze / thaw cycles
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
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别名
- SLC22A5
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背景
- Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. Alternative splicing of this gene results in multiple transcript variants.,SLC22A5,CDSP,OCTN2,Cancer,Signal Transduction,Endocrine & Metabolism,SLC22A5
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分子量
- 24 kDa/62 kDa/65 kDa
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基因ID
- 6584
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UniProt
- O76082
抗原
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