抗体

山羊抗精氨酸酶I抗体

MBS422008

0.1毫克

300美元

多克隆

山羊

未共轭

人类, 小鼠, 大鼠, 狗, 牛

免疫印迹, 酶免疫法

抗体

山羊抗精氨酸酶I抗体

精氨酸酶I

山羊抗精氨酸酶, 类型1/ARG1抗体;ARG1;精氨酸酶, 肝;HGNC:663;A-I;精氨酸酶, 类型I;精氨酸酶1;肝类型精氨酸酶;类型I精氨酸酶;ARG1抗体;精氨酸酶;肝抗体;HGNC:663抗体;A-I抗体;精氨酸酶;类型I抗体;精氨酸酶1抗体;肝类型精氨酸酶抗体;类型I精氨酸酶抗体;精氨酸酶I;精氨酸酶I

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

ARG1

ARG1;ARG1

ARGI1_HUMAN

多克隆

山羊

Tested: Human, Mouse, Rat, Pig; Expected from sequence similarity: Human, Mouse, Rat, Dog, Pig, Cow

322

CFGLAREGNHKPID

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)

Peptide ELISA: Antibody detection limit dilution 1: 64000. Western Blot: Approx.37kDa band observed in Human, Mouse, Rat and Pig Liver lysates (calculated MW of 34.7kDa according to NP_000036.2). The observed molecular weight corresponds to earlier findings with different antibodies from other commercial sources. Recommended concentration: 0.01-0.03ug/ml.

Immunogen: Peptide with sequence CFGLAREGNHKPID, from the C Terminus of the protein sequence according to NP_000036.2. Epitope: C Terminus

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); Arginine Biosynthesis Pathway (82943); Arginine Biosynthesis Pathway (306); Biosynthesis Of Amino Acids Pathway (790012); Biosynthesis Of Amino Acids Pathway (795174); IL4-mediated Signaling Events Pathway (137933)

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]

ARG1: Homotrimer. By arginine or homoarginine. Belongs to the arginase family. 3 isoforms of the human protein are produced by alternative splicing. Protein type: Amino Acid Metabolism - arginine and proline; EC 3.5.3.1; Hydrolase. Chromosomal Location of Human Ortholog: 6q23. Cellular Component: cell soma; cytoplasm; cytosol; extracellular space; mitochondrial outer membrane; neuron projection; nucleus. Molecular Function: arginase activity; manganese ion binding. Biological Process: aging; arginine catabolic process; arginine catabolic process to ornithine; collagen biosynthetic process; liver development; lung development; mammary gland involution; maternal process involved in pregnancy; positive regulation of endothelial cell proliferation; response to amine stimulus; response to amino acid stimulus; response to axon injury; response to cadmium ion; response to drug; response to herbicide; response to manganese ion; response to methylmercury; response to selenium ion; response to vitamin A; response to vitamin E; response to zinc ion; urea cycle. Disease: Argininemia

0.1毫克

300美元