catalog number :
MBS711584
products full name :
Rabbit anti-human calcium/calmodulin-dependent serine protein kinase (MAGUK family) polyclonal Antibody
products short name :
calcium/calmodulin-dependent serine protein kinase
products name syn :
calcium/calmodulin-dependent serine protein kinase (MAGUK family); CASK; CAGH39; CMG; FGS4; FLJ22219; FLJ31914; LIN2; MICPCH; TNRC8
other names :
calcium/calmodulin-dependent serine protein kinase; Peripheral plasma membrane protein CASK; peripheral plasma membrane protein CASK; hCASK; protein lin-2 homolog; trinucleotide repeat containing 8; calcium/calmodulin-dependent serine protein kinase membrane-associated guanylate kinase; calcium/calmodulin-dependent serine protein kinase (MAGUK family); Calcium/calmodulin-dependent serine protein kinase; Protein lin-2 homolog
other gene names :
CASK; CASK; CMG; FGS4; LIN2; TNRC8; CAGH39; CAMGUK; MICPCH; MRXSNA; LIN2; hCASK
uniprot entry name :
CSKP_HUMAN
reactivity :
Human, Mouse, Rat
purity :
Antigen Affinity Purified
tested application :
ELISA (EIA), Western Blot (WB)
other info1 :
Immunogen: Human CASK
other info2 :
Storage Buffer: PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20 degree C, Avoid freeze / thaw cycles.
ncbi acc num :
AAU10527.1
ncbi mol weight :
103,211 Da
ncbi pathways :
Cell-Cell Communication Pathway 477132!!Extracellular Matrix Organization Pathway 576262!!Nephrin Interactions Pathway 187228!!Non-integrin Membrane-ECM Interactions Pathway 833810!!Parkin-Ubiquitin Proteasomal System Pathway 700638!!Syndecan Interactions Pathway 833811!!Syndecan-1-mediated Signaling Events Pathway 138046!!Syndecan-2-mediated Signaling Events Pathway 138031!!Syndecan-3-mediated Signaling Events Pathway 137952!!Tight Junction Pathway 83071
ncbi summary :
This gene encodes a calcium/calmodulin-dependent serine protein kinase. The encoded protein is a MAGUK (membrane-associated guanylate kinase) protein family member. These proteins are scaffold proteins and the encoded protein is located at synapses in the brain. Mutations in this gene are associated with FG syndrome 4, mental retardation and microcephaly with pontine and cerebellar hypoplasia, and a form of X-linked mental retardation. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]