|
|
Cat. No |
Model |
Description |
Unit |
Price (VATº°µµ) |
³³±â |
Àç°í |
DataSheet |
ÁÖ¹®/°ßÀû |
LCA-24-368474 |
AP12247PU-N |
ACOX1//Human, Mouse/Rabbit |
1/EA |
|
|
|
|
¹®ÀÇ |
|
|
|
|
|
|
Subject
|
ACOX1 |
Description
|
/ Human, Mouse/Rabbit |
Clonality
|
Mono |
Company
|
Acris Antibodies GmbH |
Application
|
Enzyme Immunoassay, Western blot / Immunoblot |
Conjugation
|
|
Immunogen
|
|
Contents
|
Description: Manufacturer | Acris Antibodies GmbH | Quantity | 0.1 mg | Reactivity | Human, Mouse | Presentation | Purified | Applications | Enzyme Immunoassay, Western blot / Immunoblot | Isotype | Ig | Host | Rabbit | PDF datasheet | view | Shipping to | Worldwide | Synonyms | ACOX1, ACOX, AOX, EC 1.3.3.6, Palmitoyl-CoA oxidase, Straight-chain acyl-CoA oxidase, SCOX, Peroxisomal acyl-coenzyme A oxidase 1 | Swiss Prot Num | Q15067 | Immunogen | This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the N-terminal region of human ACOX1. | Product Type | Antibodies | Storage | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. Shelf life: one year from despatch. | References | 1. Strausberg, R.L., et al., Proc. Natl. Acad. Sci. U.S.A. 99(26):16899-16903 (2002). 2. Chu, R., et al., J. Biol. Chem. 270(9):4908-4915 (1995). 3. Aoyama, T., et al., Biochem. Biophys. Res. Commun. 198(3):1113-1118 (1994). 4. Fournier, B., et al., J. Clin. Invest. 94(2):526-531 (1994). 5. Varanasi, U., et al., Proc. Natl. Acad. Sci. U.S.A. 91(8):3107-3111 (1994). | |
Format | State: Liquid purified Ig fraction. | ? | Purification: Protein G Chromatography, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. | ? | Buffer System: PBS with 0.09% (W/V) Sodium Azide as preservative. | |
Specificity | This antibody is specific to ACOX1 (N-term). | Add. information | Calculated Molecular weight: 74442 Da | Application | ELISA: 1/1,000. Western Blot: 1/1,000. | Background | ACOX1 is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids. | Caution | This product is for research use only. Not for use in diagnostic or therapeutic procedures. | Concentration | 0.25 mg/ml | Species Reactivity | Tested: Human and Mouse. | |
|
|
|
|