G6PD purified MaxPab rabbit polyclonal antibody (D01P)
产品名称： G6PD purified MaxPab rabbit polyclonal antibody (D01P)
英文名称： G6PD purified MaxPab rabbit polyclonal antibody (D01P)
产品编号： H00002539-D01P
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Rabbit polyclonal antibody raised against a full-length human G6PD protein.
- Immunogen:
- G6PD (NP_001035810.1, 1 a.a. ~ 515 a.a) full-length human protein.
- Sequence:
- MAEQVALSRTQVCGILREELFQGDAFHQSDTHIFIIMGASGDLAKKKIYPTIWWLFRDGLLPENTFIVGYARSRLTVADIRKQSEPFFKATPEEKLKLEDFFARNSYVAGQYDDAASYQRLNSHMNALHLGSQANRLFYLALPPTVYEAVTKNIHESCMSQIGWNRIIVEKPFGRDLQSSDRLSNHISSLFREDQIYRIDHYLGKEMVQNLMVLRFANRIFGPIWNRDNIACVILTFKEPFGTEGRGGYFDEFGIIRDVMQNHLLQMLCLVAMEKPASTNSDDVRDEKVKVLKCISEVQANNVVLGQYVGNPDGEGEATKGYLDDPTVPRGSTTATFAAVVLYVENERWDGVPFILRCGKALNERKAEVRLQFHDVAGDIFHQQCKRNELVIRVQPNEAVYTKMMTKKPGMFFNPEESELDLTYGNRYKNVKLPDAYERLILDVFCGSQMHFVRSDELREAWRIFTPLLHQIELEKPKPIPYIYGSRGPTEADELMKRVGFQYEGTYKWVNPHKL
- Host:
- Rabbit
- Reactivity:
- Human
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody reactive against mammalian transfected lysate.
- MSDS:
Download
- Applications
- Western Blot (Transfected lysate)
- Western Blot analysis of G6PD expression in transfected 293T cell line (H00002539-T01) by G6PD MaxPab polyclonal antibody.
Lane 1: G6PD transfected lysate(59.30 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 2539
- GeneBank Accession#:
- NM_001042351.1
- Protein Accession#:
- NP_001035810.1
- Gene Name:
- G6PD
- Gene Alias:
- G6PD1
- Gene Description:
- glucose-6-phosphate dehydrogenase
- Omim ID:
- 305900
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
- Other Designations:
- OTTHUMP00000026034,glucose-6-phosphate 1-dehydrogenase,glucose-6-phosphate dehydrogenase, G6PD
- Related Disease
- alpha-Thalassemia
- Anemia
- Anemia, Hemolytic, Congenital Nonspherocytic
- Anemia, Sickle Cell
- Anemia, sickle cell
- beta-Thalassemia
- Birth Weight
- Cardiovascular Diseases
- Coronary Disease
- Diabetes Mellitus, Type 2
- Diabetic Ketoacidosis
- Disease Susceptibility
- Edema
- Elliptocytosis, Hereditary
- Encephalitis
- Favism
- Genetic Predisposition to Disease
- Gilbert Disease
- Glucosephosphate Dehydrogenase Deficiency