SLC22A5 抗体
-
- 抗原 See all SLC22A5 抗体
- SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This SLC22A5 antibody is un-conjugated
-
应用范围
- Immunofluorescence (IF)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human SLC22A5 (NP_003051.1).
- 亚型
- IgG
- Top Product
- Discover our top product SLC22A5 Primary Antibody
-
-
- 应用备注
- IF 1:50-1:200
- 限制
- 仅限研究用
-
- 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.
-
- 抗原
- SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
- 别名
- SLC22A5 (SLC22A5 产品)
- 别名
- CDSP antibody, OCTN2 antibody, OCTN2VT antibody, Lstpl antibody, Octn2 antibody, jvs antibody, slc22a5 antibody, MGC68932 antibody, CT1 antibody, UST2r antibody, ATOCT2 antibody, OCT2 antibody, ORGANIC CATION TRANSPORTER 2 antibody, YUP8H12R.2 antibody, YUP8H12R_2 antibody, organic cation/carnitine transporter 2 antibody, solute carrier family 22 member 5 antibody, solute carrier family 22 (organic cation transporter), member 5 antibody, solute carrier family 22 member 5 L homeolog antibody, organic cation/carnitine transporter 2 antibody, SLC22A5 antibody, Slc22a5 antibody, LOC100358417 antibody, slc22a5.L antibody, OCT2 antibody
- 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.
- 分子量
-
Observed_MW: 70kDa
Calculated_MW: 24kDa/62kDa/65kDa
- 基因ID
- 6584
- UniProt
- O76082
-