Product overview:

Carrier-free (BSA/glycerol-free) ARG1 mouse monoclonal antibody, clone LBI4E6

Field of research:

Arginine and proline metabolism, Metabolic pathways

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]

Alternative names:

OTTHUMP00000017209; arginase 1; liver-type arginase; type I arginase; arginase, liver

Species reactivity:

Human, Mouse, Rat

Host:

Mouse

Target:

ARG1

Isotype:

IgG1

Immunogen:

Full length human recombinant protein of human ARG1 (NP_000036) produced in HEK293T cell.

Clone:

LBI4E6

Conjugation:

Unconjugated

Gene name:

Homo sapiens arginase 1 (ARG1), transcript variant 2, mRNA.

Symbol:

ARG1

Pathway:

Arginine and proline metabolism, Metabolic pathways

Function:

Druggable Genome

Purification:

Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Concentration:

Form:

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Applications & dilution:

WB 1:1000~2000, IHC 1:50, FLOW 1:100

Storage buffer:

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Storage:

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

More info:

Email: info@sobekbio.com

Orders:

Email: orders@sobekbio.com