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Merck
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重要文件

L4669

Sigma-Aldrich

Anti-Lysyl Oxidase (C-terminal) antibody produced in rabbit

enhanced validation

~1 mg/mL, affinity isolated antibody, buffered aqueous solution

同義詞:

Anti-LOX, Anti-Protein lysine 6-oxidase

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

rabbit

品質等級

共軛

unconjugated

抗體表格

affinity isolated antibody

抗體產品種類

primary antibodies

無性繁殖

polyclonal

形狀

buffered aqueous solution

分子量

antigen ~50 kDa

物種活性

human

加強驗證

recombinant expression
Learn more about Antibody Enhanced Validation

濃度

~1 mg/mL

技術

western blot: 1.5-3.0 mg/mL using HEK-293T cellls expressing human LOX

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... LOX(4015)
mouse ... Lox(16948)
rat ... Lox(24914)

一般說明

The LOX gene is located on the human chromosome at 5q23.1.
The gene LOX (lysyl oxidase) encodes a copper-dependent amine oxidase that belongs to LOX family of proteins. These proteins contain highly conserved C- terminal mature catalytic domains that include the copper binding site, the lysyl tyrosyl quinine (LTQ) cofactor residues, and the cytokine receptor like (CRL) domain. It is present in both intercellular and intracellular locations.

特異性

Anti-Lysyl Oxidase (C-terminal) specifically recognizes human lysyl oxidase (LOX).

應用

Anti-Lysyl Oxidase (C-terminal) antibody produced in rabbit has been used in:
  • western blotting
  • immunofluorescence staining
  • immunohistochemistry

生化/生理作用

Altered LOX gene expression and activity are linked to skin aging and senescence. Decreased LOX gene expression and activity have been associated with severe connective tissue disorders such as Ehler-Danlos syndrome, cutis laxa, and Menkes′ syndrome. Increased LOX gene expression are associated with the development of fibrotic diseases that involve connective tissue remodeling, such as atherosclerosis, scleroderma and liver cirrhosis. LOX protein also plays an important role in breast cancer metastasis.
LOX is implicated in various intracellular functions such as the regulation of cellular differentiation, cell migration and gene transcription.
The gene LOX (lysyl oxidase) encodes an extracellular matrix remodeling enzyme that catalyzes the oxidation of primary amino group of peptidyl lysine to reactive peptidyl aldehydes. It is mainly involved in the oxidation of lysine residues in elastin and collagen, resulting in the formation of covalent cross-linkages, which stabilize these fibrous proteins. It also plays a role in several cellular processes such as developmental regulation, tumor suppression, cell motility, and cellular senescence. It is involved in hypoxia-induced metastasis and serves as a therapeutic target for the treatment of metastases.

外觀

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

儲存和穩定性

For continuous use, store at 2–8 °C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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儲存類別代碼

10 - Combustible liquids

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


分析證明 (COA)

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存取文件庫

Transdifferentiation of lung adenocarcinoma in mice with Lkb1 deficiency to squamous cell carcinoma
Han X, et al.
Nature Communications, 5(24) (2019)
Lysyl oxidase regulates breast cancer cell migration and adhesion through a hydrogen peroxide--mediated mechanism
Payne SL, et al.
Cancer Research, 65(24), 11429-11436 (2005)
Katarzyna A Cieslik et al.
Journal of molecular and cellular cardiology, 63, 26-36 (2013-07-23)
We have demonstrated that scar formation after myocardial infarction (MI) is associated with an endogenous pool of CD44(pos)CD45(neg) multipotential mesenchymal stem cells (MSC). MSC differentiate into fibroblasts secreting collagen that forms a scar and mature into myofibroblasts that express alpha
Mari Kielosto et al.
Oncotarget, 9(102), 37733-37752 (2019-02-01)
We have previously shown that proto-oncoprotein c-Jun is activated in ornithine decarboxylase (ODC)- and RAS-transformed mouse fibroblasts, and that the transformed morphology of these cells can be reversed by expressing the transactivation domain deletion mutant of c-Jun (TAM67). Here, we
AICAR-dependent AMPK activation improves scar formation in the aged heart in a murine model of reperfused myocardial infarction
Cieslik K, et al.
Journal of Molecular and Cellular Cardiology, 63(24), 26-36 (2013)

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