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- 抗原 See all SLC16A2/MCT8 (SLC16A2) 抗体
- SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))
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抗原表位
- AA 1-100
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适用
- 人
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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 SLC16A2/MCT8 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- MALQSQASEE AKGPWQEADQ EQQEPVGSPE PESEPEPEPE PEPVPVPPPE PQPEPQPLPD PAPLPELEFE SERVHEPEPT PTVETRGTAR GFQPPEGGFG
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of human SLC16A2 (NP_006508.2).
- 亚型
- IgG
- Top Product
- Discover our top product SLC16A2 Primary Antibody
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anti-Solute Carrier Family 16 Member 2 (SLC16A2) (AA 101-200) antibody
SLC16A2 适用: 人, 小鼠, 大鼠 WB, ELISA 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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- 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
- SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))
- 别名
- SLC16A2 (SLC16A2 产品)
- 别名
- MCT8 antibody, AW105741 antibody, Mct8 antibody, Xpct antibody, AHDS antibody, DXS128 antibody, DXS128E antibody, MCT 7 antibody, MCT 8 antibody, MCT7 antibody, MRX22 antibody, XPCT antibody, solute carrier family 16 member 2 antibody, solute carrier family 16 (monocarboxylic acid transporters), member 2 antibody, SLC16A2 antibody, Slc16a2 antibody
- 背景
- This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome.,SLC16A2,AHDS,DXS128,DXS128E,MCT 7,MCT 8,MCT7,MCT8,MRX22,XPCT,Signal Transduction,Cell Biology & Developmental Biology,Growth factor,Endocrine & Metabolism,Neuroscience,SLC16A2
- 分子量
- 59 kDa
- 基因ID
- 6567
- UniProt
- P36021
- 途径
- Hormone Transport
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