ARG1 monoclonal antibody
产品名称: ARG1 monoclonal antibody
英文名称: ARG1 monoclonal antibody
产品编号: H00000383-M
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:
- Mouse monoclonal antibody raised against a full-length recombinant ARG1.
- Immunogen:
- ARG1 (AAH20653.1, 1 a.a. ~ 322 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- MSAKSRTIGIIGAPFSKGQPRGGVEEGPTVLRKAGLLEKLKEQECDVKDYGDLPFADIPNDSPFQIVKNPRSVGKASEQLAGKVAEVKKNGRISLVLGGDHSLAIGSISGHARVHPDLGVIWVDAHTDINTPLTTTSGNLHGQPVSFLLKELKGKIPDVPGFSWVTPCISAKDIVYIGLRDVDPGEHYILKTLGIKYFSMTEVDRLGIGKVMEETLSYLLGRKKRPIHLSFDVDGLDPSFTPATGTPVVGGLTYREGLYITEEIYKTGLLSGLDIMEVNPSLGKTPEEVTRTVNTAVAITLACFGLAREGNHKPIDYLNPPK
- Host:
- Mouse
- Reactivity:
- Human
- Quality Control Testing:
- Antibody reactivity and specificity confirmed by ELISA and Western Blot.
- Note:
- Customer should check the viability of the hybridomas within one month from the date of receipt. Fee-for-service of long term hybridoma storage can be performed upon customer's request.
- Deliverables:
- Up to 5 positive hybridoma clones will be delivered to customer in the cryotube format.
- Application Image
- Western Blot
- ELISA
- Entrez GeneID:
- 383
- GeneBank Accession#:
- BC020653.1
- Protein Accession#:
- AAH20653.1
- Gene Name:
- ARG1
- Gene Alias:
- -
- Gene Description:
- arginase, liver
- Gene Ontology:
- Hyperlink
- Gene Summary:
- Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. [provided by RefSeq
- Other Designations:
- A-I,OTTHUMP00000017209,arginase, type I
- Related Disease
- Asthma
- Asthma
- Atherosclerosis
- Bronchiolitis, Viral
- Cardiovascular Diseases
- Coronary Disease
- Diabetes Mellitus, Type 2
- Edema
- Genetic Predisposition to Disease
- Helicobacter Infections
- Hypersensitivity
- Hypersensitivity, Immediate
- Infant, Premature, Diseases
- Inflammation
- Lung Neoplasms
- Myocardial Infarction
- Precancerous Conditions
- Pulmonary Disease, Chronic Obstructive
- Respiratory Syncytial Virus Infections