抗体

山羊抗精氨酸酶, 类型1/ARG1抗体

MBS421120

0.1毫克

290美元

多克隆

山羊

未共轭

人类, 小鼠, 狗

免疫印迹, 酶免疫法

抗体

山羊抗精氨酸酶, 类型1/ARG1抗体

精氨酸酶, 类型1/ARG1

ARG1;精氨酸酶;类型I;精氨酸酶;肝;A-I;山羊抗精氨酸酶I;精氨酸酶, 类型I;精氨酸酶, 肝;A-I;

arginase-1 isoform 2; Arginase-1; arginase-1; arginase, liver; type I arginase; liver-type arginase; arginase 1; Liver-type arginase; Type I arginase

ARG1

ARG1;ARG1

ARGI1_HUMAN

多克隆

山羊

人类, 狗, 小鼠

322

REGNHKPIDYLNPPK

通过硫酸铵沉淀和用免疫多肽抗原亲和层析从山羊血清中纯化得到的

Supplied at 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.

100ug specific antibody in 200ul

Aliquot and store at -20 degree C. Minimize freezing and thawing.

肽酶联免疫吸附测定(EIA), 免疫印迹(免疫印迹)

Western Blot: Approx 37kDa band observed in Human Liver lysates (calculated MW of 34.7kDa according to NP_000036.2. Recommended concentration: 0.01-0.03ug/ml. An anonymous customer found positive results in WB on Mouse leukaemic monocyte macrophage cells (RAW 264.7). Peptide ELISA: antibody detection limit dilution 1:2000.

Epitope: C Terminus. Immunogen: Peptide with sequence C-REGNHKPIDYLNPPK, from the C Terminus of the protein sequence according to NP_000036.2. Corresponding Immunizing Peptide: Catalog #MBS426571

Important Note: Please note that ARG1 is not expressed in Human M2 macrophages, but it is in other species (eg rodents).

10947139

NP_000036.2

NM_000045.3

25,356 Da

ATF-2 Transcription Factor Network Pathway 138006!!Amoebiasis Pathway 167324!!Amoebiasis Pathway 167191!!Arginine And Proline Metabolism Pathway 82957!!Arginine And Proline Metabolism Pathway 323!!Biosynthesis Of Amino Acids Pathway 790012!!Biosynthesis Of Amino Acids Pathway 795174!!IL4-mediated Signaling Events Pathway 137933!!Metabolic Pathways 132956!!Metabolism Pathway 477135

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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]

0.1毫克

290美元