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GALE rabbit pAb

商品貨號： PLA020216

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： GALE
蛋白名稱： GALE
Human_gene_id： 2582
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2582
Human_swiss_prot_no： Q14376
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q14376/entry
Mouse_gene_id： 74246
Mouse_gene_link： https://www.uniprot.org/uniprot/74246
Mouse_swiss_prot_no： Q8R059
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q8R059
Rat_swiss_prot_no： P18645
Rat_swiss_link： https://www.uniprot.org/uniprotkb/P18645
特異性： This antibody detects endogenous levels of GALE 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： 38kD
功能： catalytic activity:UDP-glucose = UDP-galactose.,cofactor:NAD.,disease:Defects in GALE are the cause of epimerase-deficiency galactosemia (EDG) [MIM:230350]; also known as galactosemia type 3. Clinical features include early-onset cataracts, liver damage, deafness and mental retardation. There are two clinically distinct forms of EDG. (1) A benign, or 'peripheral' form with no detectable GALE activity in red blood cells and characterized by mild symptoms. Some patients may suffer no symptoms beyond raised levels of galactose-1-phosphate in the blood. (2) A much rarer 'generalized' form with undetectable levels of GALE activity in all tissues and resulting in severe features such as restricted growth and mental development.,function:Catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine.,pathway:Carbohydrate metabolism; galactose metabolism.,similarity:Belongs to the sugar epimerase family.,subunit:Homodimer.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： cytosol,extracellular exosome,
科研貨號： PLA020216

GALE rabbit pAb

Catalog No PLA020216

Product information

基因名稱： GALE
蛋白名稱： GALE
Human_gene_id： 2582
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2582
Human_swiss_prot_no： Q14376
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q14376/entry
Mouse_gene_id： 74246
Mouse_gene_link： https://www.uniprot.org/uniprot/74246
Mouse_swiss_prot_no： Q8R059
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q8R059
Rat_swiss_prot_no： P18645
Rat_swiss_link： https://www.uniprot.org/uniprotkb/P18645
特異性： This antibody detects endogenous levels of GALE 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： 38kD
功能： catalytic activity:UDP-glucose = UDP-galactose.,cofactor:NAD.,disease:Defects in GALE are the cause of epimerase-deficiency galactosemia (EDG) [MIM:230350]; also known as galactosemia type 3. Clinical features include early-onset cataracts, liver damage, deafness and mental retardation. There are two clinically distinct forms of EDG. (1) A benign, or 'peripheral' form with no detectable GALE activity in red blood cells and characterized by mild symptoms. Some patients may suffer no symptoms beyond raised levels of galactose-1-phosphate in the blood. (2) A much rarer 'generalized' form with undetectable levels of GALE activity in all tissues and resulting in severe features such as restricted growth and mental development.,function:Catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine.,pathway:Carbohydrate metabolism; galactose metabolism.,similarity:Belongs to the sugar epimerase family.,subunit:Homodimer.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： cytosol,extracellular exosome,
科研貨號： PLA020216

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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