FITC标记的糖磷脂酰肌醇抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的糖磷脂酰肌醇抗体

FITC标记的糖磷脂酰肌醇抗体

商家询价

产品名称: FITC标记的糖磷脂酰肌醇抗体

英文名称: Anti-GPI/FITC

产品编号: HZ-10419R-FITC

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

上海沪震实业有限公司
  • 联系人 : 鲍丽雯
  • 地址 : 上海市闵行区闵北路88弄1-30号第22幢AQ136室
  • 邮编 : 200612
  • 所在区域 : 上海
  • 电话 : 139****0749 点击查看
  • 传真 : 点击查看
  • 邮箱 : www.shzbio.net
  • 二维码 : 点击查看

 Rabbit Anti-GPI/FITC Conjugated antibody 

FITC标记的糖磷脂酰肌醇抗体

 

英文名称 Anti-GPI/FITC
中文名称 FITC标记的糖磷脂酰肌醇抗体
别    名 Glucose 6 phosphate isomerase; AMF; Aurocrine motility factor; Autocrine motility factor; DKFZp686C13233; EC 5.3.1.9; G6PI_HUMAN; Glucose phosphate isomerase; Glucose-6-phosphate isomerase; GNPI; GPI; Gpi1; Hexose monophosphate isomerase; Hexosephosphate isomerase; Neuroleukin; NLK; Oxoisomerase; PHI; Phosphoglucose isomerase; Phosphohexomutase; Phosphohexose isomerase; Phosphosaccharomutase; SA 36; SA-36; SA36; Sperm antigen 36.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  细胞生物  免疫学  神经生物学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Pig, Cow, Horse, 
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 63kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Glucose 6 phosphate isomerase
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍 background:
This gene belongs to the GPI family whose members encode multifunctional phosphoglucose isomerase proteins involved in energy pathways. The protein encoded by this gene is a dimeric enzyme that catalyzes the reversible isomerization of glucose-6-phosphate and fructose-6-phosphate. The protein functions in different capacities inside and outside the cell. In the cytoplasm, the gene product is involved in glycolysis and gluconeogenesis, while outside the cell it functions as a neurotrophic factor for spinal and sensory neurons. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. [provided by RefSeq, Jul 2008].

Function:
Besides it's role as a glycolytic enzyme, mammalian GPI can function as a tumor-secreted cytokine and an angiogenic factor (AMF) that stimulates endothelial cell motility. GPI is also a neurotrophic factor (Neuroleukin) for spinal and sensory neurons.

Subunit:
Homodimer in the catalytically active form, monomer in the secreted form.

Subcellular Location:
Cytoplasm. Secreted.

Post-translational modifications:
Phosphorylation at Ser-185 by CK2 has been shown to decrease enzymatic activity and may contribute to secretion by a non-classical secretory pathway. 
ISGylated.

DISEASE:
Defects in GPI are the cause of hemolytic anemia non-spherocytic due to glucose phosphate isomerase deficiency (HA-GPID) [MIM:613470]. It is a form of anemia in which there is no abnormal hemoglobin or spherocytosis. It is caused by glucose phosphate isomerase deficiency. Severe GPI deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment.

Similarity:
Belongs to the GPI family.

Database links:

Entrez Gene: 2821 Human

Entrez Gene: 14751 Mouse

Omim: 172400 Human

SwissProt: P06744 Human

SwissProt: P06745 Mouse

Unigene: 466471 Human

Unigene: 589 Mouse



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

该基因属于GPI家族,其成员编码参与能量途径的多功能磷酸葡萄糖异构酶蛋白。该基因编码的蛋白质是催化葡萄糖-6-磷酸和果糖-6-磷酸可逆异构化的二聚酶。蛋白质在细胞内外的不同能力发挥作用。在细胞质中,基因产物参与糖酵解和糖异生,而在细胞外,它作为脊髓和感觉神经元的神经营养因子发挥作用。该基因的缺陷是导致非球形溶血性贫血的原因,严重的酶缺乏可能与胎儿水肿、新生儿立即死亡和神经功能损害有关。[ RefSeq,JUL 2008 ]提供。