Myoglobin anticorps

N° du produit ABIN966633

Cet anticorps anti-Myoglobin est un anticorps Monoclonal détectant Myoglobin dans WB, IHC et ELISA. Adapté pour Humain. Ce Primary Antibody a été cité dans 2+ publications.

Aperçu rapide pour Myoglobin anticorps (ABIN966633)

Antigène: Myoglobin (MB)

Reactivité: Humain

Hôte: Veuillez nous consulter SVP

Clonalité: Monoclonal

Conjugué: Cet anticorp Myoglobin est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Détail du produit anti-Myoglobin anticorps

Specificité: Ni-NTA purified truncated recombinant Myoglobin expressed in E. Coli strain BL21 (DE3)

Isotype: IgG1

Information d'application

Indications d'application: Western Blot: 1: 500- 1: 2,000
IHC(P): 1: 500- 1: 2,000
IHC(F): 1: 500- 1: 2,000
ELISA: Propose dilution 1: 10,000.
Determining optimal working dilutions by titration test.

Restrictions: For Research Use only

Stockage

Stock: -20 °C

Références pour anticorps anti-Myoglobin (ABIN966633)

Flögel, Laussmann, Gödecke, Abanador, Schäfers, Fingas, Metzger, Levkau, Jacoby, Schrader: "Lack of myoglobin causes a switch in cardiac substrate selection." dans: Circulation research, Vol. 96, Issue 8, pp. e68-75, (2005) (PubMed).

Ordway, Garry: "Myoglobin: an essential hemoprotein in striated muscle." dans: The Journal of experimental biology, Vol. 207, Issue Pt 20, pp. 3441-6, (2004) (PubMed).

Détails sur Myoglobin

Antigène: Myoglobin (MB)

Autre désignation: Myoglobin

Sujet: Myoglobin (MB), with 154-amino acid protein (about 17kDa), is a member of the globin superfamily and expression of myoglobin is highest in skeletal and cardiac muscle. Functionally, myoglobin is well accepted as an O2-storage protein in muscle, capable of releasing O2 during periods of hypoxia or anoxia. Myoglobin is also thought to buffer intracellular O2 concentration when muscle activity increases and to facilitate intracellular O2 diffusion by providing a parallel path that augments simple diffusion of dissolved O2. Furthermore, myoglobin is used together with cTnI or cTnT in clinical practise for better specificity in AMI diagnosis.

ID gène: 4151

Pathways: Brown Fat Cell Differentiation