Vergleich

Tropomyosin [SPM224]

ArtNr 20-272-191508
Hersteller GENWAY
Menge 0.5 ml
Kategorie
Typ Antibody
Applikationen IF, IHC
Clon SPM224
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-33C877
Similar products 20-272-191508
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Genway ID:
GWB-33C877
Clone:
SPM224
Isotype:
IgG1Light chain: kappa
Immunogen:
Full length native protein (purified) (Chicken).
Antigen Species:
Chicken
Positive Control:
Skeletal or cardiac muscle
Target:
Tropomyosin
Localization:
Cytoplasmic
Concentration:
0. 1 mg/ml Storage
Buffer:
Phosphate-buffered saline pH 7. 4 containing BSA and sodium azide
Application Note:
For IF: Use at an assay dependent dilution. For IHC-P: Use at a dilution of 1:50. Staining of formalin-fixed tissues requires boiling tissue sections in 10mM citrate buffer pH 6. 0 for 10 min followed by cooling at RT for 20 min. Not tested in other applications. Optimal dilutions/concentrations should be determined by the researcher. Cellular
Localization:
Cytoplasmic Tropomyosin is a dimeric coiled-coil protein that binds along the length of actin filaments. It is associated with the thin filaments of muscle cells and the microfilaments of nonmuscle cells. Chicken embryo fibroblasts (CEF) contain five isoforms of tropomyosin (a b 1 2 and 3) identified as such by their different apparent molecular masses after separation by SDS-PAGE but similar biochemical properties such as resistance to heat and organic solvents the ability to bind to F-actin filaments and the lack of proline and tryptophan.
Function:
Binds to actin filaments in muscle and non-muscle cells. Plays a central role in association with the troponin complex in the calcium dependent regulation of vertebrate striated muscle contraction. Smooth muscle contraction is regulated by interaction with caldesmon. In non-muscle cells is implicated in stabilizing cytoskeleton actin filaments.
Subunit:
Heterodimer of an alpha and a beta chain.
Subcellular Location:
Cytoplasm cytoskeleton.
Tissue Specificity:
Detected in primary breast cancer tissues but undetectable in normal breast tissues in Sudanese patients. Isoform 1 is expressed in adult and fetal skeletal muscle and cardiac tissues with higher expression levels in the cardiac tissues. Isoform 10 is expressed in adult and fetal cardiac tissues but not in skeletal muscle.
Domain:
The molecule is in a coiled coil structure that is formed by 2 polypeptide chains. The sequence exhibits a prominent seven-residues periodicity. Mass Spectrometry: Mass=32875. 93; Method=MALDI; Range=1-284 (P09493-3); Source=PubMed:11840567; .
Disease:
Defects in TPM1 are the cause of cardiomyopathy familial hypertrophic type 3 (CMH3) [MIM:115196]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea syncope collapse palpitations and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
Disease:
Defects in TPM1 are the cause of cardiomyopathy dilated type 1Y (CMD1Y) [MIM:611878]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.
Similarity:
Belongs to the tropomyosin family.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

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