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HEM6 rabbit pAb
商品货号: PLA020054
适 应 性: 人,小鼠,大鼠
WB
¥600元
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MSDS
说明书
商品描述
  • 基因名称: CPOX CPO CPX
  • 蛋白名称: HEM6
  • Human_gene_id: 1371
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1371
  • Human_swiss_prot_no: P36551
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P36551/entry
  • Mouse_gene_id: 12892
  • Mouse_gene_link: https://www.uniprot.org/uniprot/12892
  • Mouse_swiss_prot_no: P36552
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P36552
  • Rat_gene_id: 304024
  • Rat_gene_link: https://www.uniprot.org/uniprot/304024
  • Rat_swiss_prot_no: Q3B7D0
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/Q3B7D0
  • 特异性: This antibody detects endogenous levels of HEM6 at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 50kD
  • 功能: catalytic activity:Coproporphyrinogen-III + O(2) + 2 H(+) = protoporphyrinogen-IX + 2 CO(2) + 2 H(2)O.,disease:Defects in CPOX are the cause of hereditary coproporphyria (HCP) [MIM:121300]. HCP is an acute hepatic porphyria and an autosomal dominant disease characterized by neuropsychiatric disturbances and skin photosensitivity. Biochemically, there is an overexcretion of coproporphyrin III in the urine and in the feces. HCP is clinically characterized by attacks of abdominal pain, neurological disturbances, and psychiatric symptoms. The symptoms are generally manifested with rapid onset, and can be precipitated by drugs, alcohol, caloric deprivation, infection, endocrine factors or stress. A severe variant form is harderoporphyria, which is characterized by earlier onset attacks, massive excretion of harderoporphyrin in the feces, and a marked decrease of coproporphyrinogen IX oxidase activity.,pathway:Porphyrin metabolism; protoporphyrin-IX biosynthesis; protoporphyrinogen-IX from coproporphyrinogen-III (O2 route): step 1/1.,similarity:Belongs to the aerobic coproporphyrinogen-III oxidase family.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Mitochondrion intermembrane space.
  • 科研货号: PLA020054
HEM6 rabbit pAb
Catalog No PLA020054
Product information
  • 基因名称: CPOX CPO CPX
  • 蛋白名称: HEM6
  • Human_gene_id: 1371
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1371
  • Human_swiss_prot_no: P36551
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P36551/entry
  • Mouse_gene_id: 12892
  • Mouse_gene_link: https://www.uniprot.org/uniprot/12892
  • Mouse_swiss_prot_no: P36552
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/P36552
  • Rat_gene_id: 304024
  • Rat_gene_link: https://www.uniprot.org/uniprot/304024
  • Rat_swiss_prot_no: Q3B7D0
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/Q3B7D0
  • 特异性: This antibody detects endogenous levels of HEM6 at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 50kD
  • 功能: catalytic activity:Coproporphyrinogen-III + O(2) + 2 H(+) = protoporphyrinogen-IX + 2 CO(2) + 2 H(2)O.,disease:Defects in CPOX are the cause of hereditary coproporphyria (HCP) [MIM:121300]. HCP is an acute hepatic porphyria and an autosomal dominant disease characterized by neuropsychiatric disturbances and skin photosensitivity. Biochemically, there is an overexcretion of coproporphyrin III in the urine and in the feces. HCP is clinically characterized by attacks of abdominal pain, neurological disturbances, and psychiatric symptoms. The symptoms are generally manifested with rapid onset, and can be precipitated by drugs, alcohol, caloric deprivation, infection, endocrine factors or stress. A severe variant form is harderoporphyria, which is characterized by earlier onset attacks, massive excretion of harderoporphyrin in the feces, and a marked decrease of coproporphyrinogen IX oxidase activity.,pathway:Porphyrin metabolism; protoporphyrin-IX biosynthesis; protoporphyrinogen-IX from coproporphyrinogen-III (O2 route): step 1/1.,similarity:Belongs to the aerobic coproporphyrinogen-III oxidase family.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Mitochondrion intermembrane space.
  • 科研货号: PLA020054
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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