HBA1 (Human) Recombinant Protein (Q01)
产品名称: HBA1 (Human) Recombinant Protein (Q01)
英文名称: HBA1 (Human) Recombinant Protein (Q01)
产品编号: H00003039-Q01
产品价格: 0
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围: null
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
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- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Human HBA1 partial ORF ( NP_000549, 33 a.a. - 142 a.a.) recombinant protein with GST-tag at N-terminal.
- Sequence:
- MFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPAVHASLDKFLASVSTVLTSKYR
- Theoretical MW (kDa):
- 37.84
- Preparation Method:
- in vitro wheat germ expression system
- Purification:
- Glutathione Sepharose 4 Fast Flow
- Storage Buffer:
- 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
- Storage Instruction:
- Store at -80°C. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- 12.5% SDS-PAGE Stained with Coomassie Blue.
- Note:
- Best use within three months from the date of receipt of this protein.
- MSDS:
- Download
- Application Image
- Enzyme-linked Immunoabsorbent Assay
- Western Blot (Recombinant protein)
- Antibody Production
- Protein Array
- Entrez GeneID:
- 3039
- GeneBank Accession#:
- NM_000558
- Protein Accession#:
- NP_000549
- Gene Name:
- HBA1
- Gene Alias:
- CD31,MGC126895,MGC126897
- Gene Description:
- hemoglobin, alpha 1
- Omim ID:
- 141800
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported. [provided by RefSeq
- Other Designations:
- alpha 1 globin,alpha one globin,alpha-1 globin,alpha-1-globin,hemoglobin alpha 1 globin chain,hemoglobin alpha-1 chain
- Related Disease
- Abortion, Spontaneous
- Albuminuria
- alpha-Thalassemia
- Anemia
- Anemia, Aplastic
- Anemia, Hypochromic
- Anemia, Sickle Cell
- Anemia, sickle cell
- beta-Thalassemia
- Dyslipidemias
- Fetal Diseases
- Genetic Predisposition to Disease
- Glucosephosphate Dehydrogenase Deficiency
- Hemolysis
- Hypertension, Pulmonary
- Iron Overload
- Malaria
- Malaria, Cerebral
- Malaria, Falciparum