Elabscience

ARG1 / Arginase 1 Polyclonal Antibody

Product Code:
 
E-AB-68336
Product Group:
 
Primary Antibodies
Supplier:
 
Elabscience
Host Type:
 
Rabbit
Antibody Isotype:
 
IgG
Antibody Clonality:
 
Polyclonal
Regulatory Status:
 
RUO
Target Species:
  • Human
  • Mouse
  • Rat
Applications:
  • Immunofluorescence (IF)
  • Western Blot (WB)
Shipping:
 
Ice packs
Storage:
 
Store at -20°C. Avoid freeze / thaw cycles.
1 / 2
Western blot analysis of HepG2 using Arginase1 (ARG1) Polyclonal Antibody at 1:400 dilution.
2 / 2
Immunofluorescence analysis of human liver cancer cells using Arginase 1 (ARG1) Polyclonal Antibody at dilution of 1:50 (40x lens). Blue: DAPI for nuclear staining.
❮❯

Western blot analysis of HepG2 using Arginase1 (ARG1) Polyclonal Antibody at 1:400 dilution.
Immunofluorescence analysis of human liver cancer cells using Arginase 1 (ARG1) Polyclonal Antibody at dilution of 1:50 (40x lens). Blue: DAPI for nuclear staining.

No additional charges, what you see is what you pay! *

CodeSizePrice
E-AB-68336-60uL60uL£210.00
Quantity:
E-AB-68336-120uL120uL£291.00
Quantity:
E-AB-68336-200uL200uL£431.00
Quantity:
Prices exclude any Taxes / VAT
How to order with us   Contact us
Stay in control of your spending. These prices have no additional charges, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: China.
Typical lead time: 14-21 working days.
Contact us for more accurate information.
  • Further Information
  • Documents
  • Show All

Further Information

Abbreviation:
ARG1 / Arginase 1
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.
Buffer:
PBS with 0.05% proclin300,50% glycerol,pH7.3.
Calculated MW:
25kDa/34kDa/35kDa
Concentration:
1 mg/mL
Conjugation:
Unconjugated
Dilution:
WB 1:500-1:2000,IF 1:50-1:200
Immunogen:
Recombinant fusion protein of human ARG1 / Arginase 1
ObservedMW:
40KDa
Purification method:
Affinity purification
Target Synonym:
ARG1;arginase-1
UNIProt ID:
P05089

Documents