GeneTex
United States (US)

Arginase 1 antibody, C-term

GTX88484_551_IHC-P_18122102_249.jpg
GTX88484_1627_WB_18122102_775.jpg
GTX88484_1628_WB_18122102_293.jpg
GTX88484_550_IHC-P_18122102_452.jpg

Cat No. GTX88484

Host Goat
Clonality Polyclonal
Isotype IgG
Application WB, IHC-P
Reactivity Human, Mouse, Rat, Pig
APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application Dilution
WB 0.01-0.03μg/ml
IHC-P 3.75μg/ml

Note :

IHC-P
Human Kidney shows preferential staining of PCT.

Not tested in other applications.

Calculated MW

35 kDa. ( Note )

Positive Control

The peptide used to generate this antibody is available for purchase (GTX88484-PEP).

Predict Reactivity

Bovine, Dog(>80% identity)
PROPERTIES

Form

Liquid

Buffer

Tris saline pH7.3, 0.02% sodium azide, 0.5% BSA.

Storage

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

Concentration

0.50 mg/ml (Please refer to the vial label for the specific concentration.)

Antigen Species

Human

Immunogen

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

Purification

Purified by ammonium sulphate precipitation followed by antigen affinity chromatography

Conjugation

Unconjugated

Note

For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
TARGET

Synonyms

Arginase 1,Arg1

Background

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]

Database

Research Area

DATA IMAGES
GTX88484_551_IHC-P_18122102_249.jpg

GTX88484 IHC-P Image

IHC-P analysis of human kidney using GTX88484 Arginase 1 antibody, C-term.
Antigen retrieval : Tris/EDTA buffer pH 9
Dilution : 4µg/ml

GTX88484_1627_WB_18122102_775.jpg

GTX88484 WB Image

WB analysis of human liver lysate using GTX88484 Arginase 1 antibody, C-term.
Dilution : 0.01µg/ml
Loading : 35µg protein in RIPA buffer

GTX88484_1628_WB_18122102_293.jpg

GTX88484 WB Image

WB analysis of pig (A), mouse (B) and rat (C) liver lysates using GTX88484 Arginase 1 antibody, C-term.
Dilution : 0.03µg/ml
Loading : 35µg protein in RIPA buffer

GTX88484_550_IHC-P_18122102_452.jpg

GTX88484 IHC-P Image

IHC-P analysis of human liver using GTX88484 Arginase 1 antibody, C-term.
Antigen retrieval : citrate buffer pH 6
Dilution : 3.75µg/ml

Package List Price ($)
$ 329