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兔甲状腺球蛋白抗体
产品名称:
兔甲状腺球蛋白抗体
英文名称:
TG
产品类别:
抗体
产品编号:
Ys-0291R
产品应用:
ELISA IHC-P IHC-F IF
性状:
Liquid
纯化方法:
affinity purified by Protein A
保质期:
12个月
保存条件:
Shipped at 4℃. Store at -20 °C for one year. Avoid
[价格]
规格 价格 库存
50ul ¥ 1200 8
100ul ¥ 1900 6
200ul ¥ 2900 2

产品详情

 

产品编号 Ys-0291R
英文名称 TG
中文名称 甲状腺球蛋白抗体
别    名 THYG_HUMAN; Thyroglobulin; AITD 3; AITD3; hTG; TDH3; Tgn;  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Rat,  (predicted: Human, Mouse, Dog, Pig, Cow, Cat, )
产品应用 ELISA=1:2000-10000 IHC-P=1:200-1000 IHC-F=1:200-1000 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 660kDa
细胞定位 分泌型蛋白 
性    状 Liquid
浓    度 2mg/1ml
免 疫 原 Thyroglobulin protein: full length 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 Thyroglobulin (Tg) is a glycoprotein homodimer produced predominantly by the thryroid gland. It acts as a substrate for the synthesis of thyroxine and triiodothyronine as well as the storage of the inactive forms of thyroid hormone and iodine. Thyroglobulin is secreted from the endoplasmic reticulum to its site of iodination, and subsequent thyroxine biosynthesis, in the follicular lumen. Mutations in this gene cause thyroid dyshormonogenesis, manifested as goiter, and are associated with moderate to severe congenital hypothyroidism. Polymorphisms in this gene are associated with susceptibility to autoimmune thyroid diseases (AITD) such as Graves disease and Hashimoto thryoiditis. [provided by RefSeq, Nov 2009]

Function:
Precursor of the iodinated thyroid hormones thyroxine (T4) and triiodothyronine (T3).

Subunit:
Homodimer.

Subcellular Location:
Secreted.

Tissue Specificity:
Thyroid gland specific.

Post-translational modifications:
Sulfated tyrosines are desulfated during iodination.

DISEASE:
Defects in TG are the cause of thyroid dyshormonogenesis 3 (TDH3) [MIM:274700]. A disorder due to thyroid dyshormonogenesis, causing large goiters of elastic and soft consistency in the majority of patients. Although the degree of thyroid dysfunction varies considerably among patients with defective thyroglobulin synthesis, patients usually have a relatively high serum free triiodothyronine (T3) concentration with disproportionately low free tetraiodothyronine (T4) level. The maintenance of relatively high free T3 levels prevents profound tissue hypothyroidism except in brain and pituitary, which are dependent on T4 supply, resulting in neurologic and intellectual defects in some cases.
Variations in TG are associated with susceptibility to autoimmune thyroid disease type 3 (AITD3) [MIM:608175]. AITDs including Graves disease (GD) and Hashimoto thyroiditis (HT), are among the most common human autoimmune diseases. They are complex diseases, which are caused by an interaction between susceptibility genes and nongenetic factors, such as infection.

Similarity:
Belongs to the type-B carboxylesterase/lipase family.
Contains 11 thyroglobulin type-1 domains.

SWISS:
P01266

Gene ID:
7038

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