SNAP91 anticorps
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- Antigène Voir toutes SNAP91 Anticorps
- SNAP91 (Synaptosomal-Associated Protein 91 (SNAP91))
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Reactivité
- Humain, Rat, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SNAP91 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human CALM2
- Isotype
- IgG
- Top Product
- Discover our top product SNAP91 Anticorps primaire
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- Indications d'application
- WB 1:500 - 1:2000
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- SNAP91 (Synaptosomal-Associated Protein 91 (SNAP91))
- Autre désignation
- CALM (SNAP91 Produits)
- Synonymes
- anticorps AP180, anticorps CALM, anticorps Ap180, anticorps 91kDa, anticorps F1-20, anticorps mKIAA0656, anticorps synaptosome associated protein 91, anticorps synaptosomal-associated protein, 91kDa homolog, anticorps synaptosomal-associated protein 91, anticorps SNAP91, anticorps LOC100147907, anticorps Snap91
- Sujet
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Synonyms: CALM 1,CALM 2,CALM 3,CALM,CALM,CALM1,CALM2,Calm3,CALML2,calmodulin 1 (phosphorylase kinase,delta),Calmodulin 2 (phosphorylase kinase,delta),Calmodulin 3 (phosphorylase kinase,delta),Calmodulin,CaM,CAM I,CAM1,CAM2,CAM3,CAMB,CAMC,CAMI,CAMII,CPVT4,DD132,FLJ99410,LP7057 protein,PHKD,PHKD2,PHKD3,phosphorylase kinase delta,phosphorylase kinase,delta subunit
Background: 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.
- Poids moléculaire
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Observed_MW: 15kDa
Calculated_MW: 17kDa
- ID gène
- 801
- UniProt
- P62158
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