MYBPC1 anticorps (AA 51-150) (Alexa Fluor 350)

N° du produit ABIN1388877

Détail du produit anti-MYBPC1 anticorps (Alexa Fluor 350)

Antigène: MYBPC1 (Myosin Binding Protein C, Slow Type (MYBPC1))

Épitope: AA 51-150

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MYBPC1 est conjugé à/à la Alexa Fluor 350

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse,Rat,Dog,Sheep,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human MYBPC1

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur MYBPC1

Antigène: MYBPC1 (Myosin Binding Protein C, Slow Type (MYBPC1))

Autre désignation: MYBPC1 (MYBPC1 Produits)

Synonymes: anticorps MYBPC1, anticorps zgc:92073, anticorps LCCS4, anticorps MYBPCC, anticorps MYBPCS, anticorps 8030451F13Rik, anticorps myosin binding protein C, slow type, anticorps myosin binding protein C, slow-type, anticorps MYBPC1, anticorps mybpc1, anticorps Mybpc1

Sujet:

Synonyms: skeletal muscle slow isoform, slow-type, C protein, skeletal muscle slow isoform, C-protein, MYBPC1, MYBPCC, MYBPCS, Myosin binding protein C, slow type, Myosin-binding protein C, MYPC1_HUMAN, skeletal muscle C protein, Slow MyBP C, Slow MyBP-C.

Background: MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.