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HEM6 rabbit pAb

商品貨號(hào)： PLA020054

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： CPOX CPO CPX
蛋白名稱： 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
特異性： This antibody detects endogenous levels of HEM6 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1：500-2000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Mitochondrion intermembrane space.
科研貨號(hào)： PLA020054

HEM6 rabbit pAb

Catalog No PLA020054

Product information

基因名稱： CPOX CPO CPX
蛋白名稱： 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
特異性： This antibody detects endogenous levels of HEM6 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1：500-2000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Mitochondrion intermembrane space.
科研貨號(hào)： PLA020054

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.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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