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SLC16A2/MCT8 蛋白

(Solute Carrier Family 16 Member 2 (SLC16A2))
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. [provided by RefSeq, Mar 2012].

2 results :

SLC16A2 宿主: 人 宿主: 大肠杆菌(E. Coli) Recombinant ELISA, SDS, WB
产品编号 ABIN7579527
 
SLC16A2 宿主: 人 宿主: 小麦胚 Recombinant AP
产品编号 ABIN1330488
 
  • 类型 Protein
    • Protein
  • 应用范围
    • Affinity Purification (AP)
    • ELISA
    • SDS-PAGE (SDS)
    • Western Blotting (WB)
  • 适用
    • Human
  • Carrier free only
  • 抗体来源
    • Escherichia coli (E. coli)
    • Wheat germ
  • 标记
    • His-SUMO Tag
    • 非结合性
  • 蛋白类型
    • Recombinant
  • Format
    • Liquid
    • Lyophilized
  • Supplier
    • antibodies-online

Aliases for SLC16A2/MCT8 蛋白

solute carrier family 16 member 2 (SLC16A2) 蛋白
solute carrier family 16 (monocarboxylic acid transporters), member 2 (Slc16a2) 蛋白
solute carrier family 16 member 2 (Slc16a2) 蛋白
AHDS 蛋白
AW105741 蛋白
DXS128 蛋白
DXS128E 蛋白
MCT 7 蛋白
MCT7 蛋白
MCT8 蛋白
Mct8 蛋白
MCT 8 蛋白
MRX22 蛋白
Xpct 蛋白
XPCT 蛋白
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