日韩成人无码毛片,成人无码A级毛片免费播放,精品乱码一区内射人妻无码,强伦轩人妻一区二区三区四区,欧美一级婬片AAAAAAA欠钱,亚洲精品乱码久久久久久蜜桃91,中文在线字幕免费观看,免费看无码一级A片放24小时 ,精品人妻少妇嫩草AV无码专区,99人妻碰碰碰久久久久禁片,国内精品一区二区,老熟妇欲乱AV无码 ,国产69精品久久久久久久久久久久,www.17c路com,国产成人在线视频,91久久精品国自产合

最近搜索:細(xì)胞培養(yǎng) 微生物學(xué) 分子生物 生物化學(xué)
首頁(yè)>>免疫學(xué)>>一抗>>磷酸半乳糖尿苷酸轉(zhuǎn)移酶1抗體
磷酸半乳糖尿苷酸轉(zhuǎn)移酶1抗體
  • 產(chǎn)品貨號(hào):
    BN40986R
  • 中文名稱:
    磷酸半乳糖尿苷酸轉(zhuǎn)移酶1抗體
  • 英文名稱:
    Rabbit anti-GALT Polyclonal antibody
  • 品牌:
    Biorigin
  • 貨號(hào)

    產(chǎn)品規(guī)格

    售價(jià)

    備注

  • BN40986R-100ul

    100ul

    ¥2360.00

    交叉反應(yīng):Mouse,Rat(predicted:Human,Cow) 推薦應(yīng)用:WB,IHC-P,IHC-F,ELISA

  • BN40986R-200ul

    200ul

    ¥3490.00

    交叉反應(yīng):Mouse,Rat(predicted:Human,Cow) 推薦應(yīng)用:WB,IHC-P,IHC-F,ELISA

產(chǎn)品描述

英文名稱GALT
中文名稱磷酸半乳糖尿苷酸轉(zhuǎn)移酶1抗體
別    名Gal 1 P uridylyltransferase; Galactose 1 phosphate uridyl transferase; Galactose 1 phosphate uridylyltransferase; UDP glucose hexose 1 phosphate uridylyltransferase; GALT_HUMAN.  
研究領(lǐng)域腫瘤  細(xì)胞生物  免疫學(xué)  激酶和磷酸酶  
抗體來(lái)源Rabbit
克隆類型Polyclonal
交叉反應(yīng)Mouse, Rat,  (predicted: Human, Cow, )
產(chǎn)品應(yīng)用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 (石蠟切片需做抗原修復(fù))
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量43kDa
細(xì)胞定位細(xì)胞漿 
性    狀Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human GALT:251-350/379 
亞    型IgG
純化方法affinity purified by Protein A
儲(chǔ) 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
產(chǎn)品介紹GALT (Galactose 1 phosphate uridyl transferase) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP glucose + galactose 1 phosphate to glucose 1 phosphate + UDP galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined.

Subunit:
Homodimer (Probable).

DISEASE:
Defects in GALT are the cause of galactosemia (GALCT) [MIM:230400]. Galactosemia is an inherited disorder of galactose metabolism that causes jaundice, cataracts, and mental retardation.

Similarity:
Belongs to the galactose-1-phosphate uridylyltransferase type 1 family.

SWISS:
P07902

Gene ID:
2592

Database links:

Entrez Gene: 2592 Human

Entrez Gene: 14430 Mouse

Entrez Gene: 298003 Rat

Omim: 606999 Human

SwissProt: P07902 Human

SwissProt: Q03249 Mouse

SwissProt: P43424 Rat

Unigene: 522090 Human

Unigene: 439669 Mouse

Unigene: 102781 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.


轮台县| 雅江县| 双江| 通江县| 浪卡子县| 曲靖市| 旬邑县| 辛集市| 彭阳县| 阿尔山市| 水城县| 洛隆县| 景宁| 合山市| 河间市| 东至县| 靖边县| 吐鲁番市| 江北区| 富民县| 汉寿县| 霍林郭勒市| 武穴市| 浦东新区| 崇文区| 遵义县| 闽清县| 和龙市| 且末县| 金门县| 拜城县| 扶余县| 凭祥市| 科尔| 东平县| 甘德县| 盖州市| 莱阳市| 连云港市| 祁门县| 珲春市|