Calmodulin antibody [J4D8]

Eine Lieferung in diese Region ist nicht möglich.

SKU:: GTX57543
Zusätzliche Namen:: calmodulin 2 , CALM2 , CAMII , LQT15 , PHKD , PHKD2 , caM , Calmodulin 2
Anwendung:: Flow Cytometry, WB, IF, ICC
Konzentration:: 1 mg/ml
Physischer Zustand:: Liquid
Spezies-Reaktivität:: Human
Aufreinigung:: Protein G Purified
Lagerbedingungen:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:: Genetex
Host:: Mouse
Reaktivitäten:: Human, Mouse
Buffer:: PBS, 10% Glycerol, 0.02% Sodium azide.
Immunogen:: The clone J4D8 is derived from hybridization of mouse F2 myeloma cells with spleen cells from BALB/c mice immunized with a recombinant human Calmodulin protein.
Klon:: J4D8
Uniprot:: P0DP23, P0DP24, P0DP25, P62158
Synonyme:: CALM;CALML2;calmodulin 1 (phosphorylase kinase, delta);calmodulin 2 (phosphorylase kinase, delta);calmodulin-1;Calmodulin-2;Calmodulin-3;caM;CAM1;CAM2;CAM3;CAMB;CAMC;CAMI;CAMII;CAMIII;CPVT4;CPVT6;DD132;epididymis secretory protein Li 72;HEL-S-72;LP7057 protein;LQT14;LQT15;LQT16;PHKD;PHKD2;PHKD3;phosphorylase kinase delta;phosphorylase kinase subunit delta;phosphorylase kinase, delta subunit;prepro-calmodulin 1;prepro-calmodulin 2;prepro-calmodulin 3
Weitere Details:: This gene is a member of the calmodulin gene family. There are three distinct calmodulin genes dispersed throughout the genome that encode the identical protein, but differ at the nucleotide level. Calmodulin is a calcium binding protein that plays a role in signaling pathways, cell cycle progression and proliferation. Several infants with severe forms of long-QT syndrome (LQTS) who displayed life-threatening ventricular arrhythmias together with delayed neurodevelopment and epilepsy were found to have mutations in either this gene or another member of the calmodulin gene family (PMID:23388215). Mutations in this gene have also been identified in patients with less severe forms of LQTS (PMID:24917665), while mutations in another calmodulin gene family member have been associated with catecholaminergic polymorphic ventricular tachycardia (CPVT)(PMID:23040497), a rare disorder thought to be the cause of a significant fraction of sudden cardiac deaths in young individuals. Pseudogenes of this gene are found on chromosomes 10, 13, and 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]

Versandbedingungen:: Blue Ice