CDKL5 rabbit pAb
This gene is a member of Ser/Thr protein kinase family and encodes a phosphorylated protein with protein kinase activity. Mutations in this gene have been associated with X-linked infantile spasm syndrome (ISSX), also known as X-linked West syndrome, and Rett syndrome (RTT). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008],
Product Specifications
Background
Gene ID
6792
UniProt
O76039
Cellular Locus
Nucleus. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome.
Host
Rabbit
Species Reactivity
Human,Mouse
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human protein . at AA range: 30-110
Clonality
Polyclonal
Isotype
IgG
Source
Rabbit
Applications
WB, ELISA
Validated Applications
WB,ELISA
Stability
-20°C/1 year
Concentration
1 mg/mL
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Molecular Weight
113kD
Storage Conditions
PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.
Product Datasheet
https://www.elkbiotech.com/upload/file/Antibodies/pAb/ES9030-1.pdf
Observed Molecular Weight
113 kD
Subcellular Location
Nucleus . Cytoplasm, cytoskeleton, cilium basal body . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome .
Gene ID (Human)
6792
SwissProt (Human)
O76039
Available Sizes
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items
MLLT6 (Protein AF-17, ALL1-fused Gene from Chromosome 17 Protein, AF17, FLJ23480) (MaxLight 405)
MLLT6 (Protein AF-17, ALL1-fused Gene from Chromosome 17 Protein, AF17, FLJ23480) (MaxLight 405)
