SLC16A2/MCT8 抗体 (N-Term)
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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
- N-Term
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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
- EPEPVPVPPP EPQPEPQPLP DPAPLPELEF ESERVHEPEP TPTVETRGTA
- 纯化方法
- Affinity purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the N terminal region of human SLC16A2
- 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
anti-Solute Carrier Family 16 Member 2 (SLC16A2) (Internal Region) antibodySLC16A2 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 16 Member 2 (SLC16A2) (AA 1-100) antibodySLC16A2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- Optimal working dilution should be determined by the investigator.
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent 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
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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.
Alias Symbols: AHDS, MCT7, MCT8, XPCT, MCT 7, MCT 8, MRX22, DXS128, DXS128E
Protein Size: 539 - 基因ID
- 6567
- NCBI登录号
- NM_006517, NP_006508
- UniProt
- P36021
- 途径
- Hormone Transport
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