CAMKI (Protein|Antibody|cDNA Clone|ELISA Kit)

All CAMKI reagents are produced in house and quality controlled, including 2 CAMKI Antibody, 16 CAMKI Gene, 1 CAMKI IPKit, 1 CAMKI Protein, 1 CAMKI qPCR. All CAMKI reagents are ready to use.

Recombinant CAMKI proteins are expressed by E. coli with fusion tags as N-cleavage.

CAMKIantibodies are validated with different applications, which are ELISA, WB, IP.

CAMKIcDNA clones are full length sequence confirmed and expression validated. There are 13 kinds of tags for each CAMKI of different species, especially GFP tag, OFP tag, FLAG tag and so on. There are three kinds of vectors for choice, cloning vector, expression vector and lentivrial expression vector.

CAMKI Protein (1)


CAMKI Protein, Human, Recombinant


Expression host: E. coli

Human CAMKI/CAMK1 Protein 9890

CAMKI Antibody (2)

Application Clonality

Anti-CAMKI Antibody


Application: WB,ELISA,IP

Clonality: PAb

Human CAMKI/CAMK1 Immunoprecipitation(IP) 8112

Anti-CAMKI Antibody


Application: ELISA

Clonality: MAb


CAMKI cDNA Clone (16)


CAMKI qPCR Primer (1)

CAMKI IP Kit (1)

Calcium/calmodulin-dependent protein kinase or CaM kinases are serine/threonine-specific protein kinases that are primarily regulated by the Calcium/calmodulin complex. These kinases show a memory effect on activation. CaM kinases activity can outlast the intracellular calcium transient that is needed to activate it. In neurons, this property is important for the induction of synaptic plasticity. Pharmacological inhibition of CaM kinases II blocks the induction of long-term potentiation. Upon activation, CaM kinases II phosphorylates postsynaptic glutamate receptors and changes the electrical properties of the synapse.

Calcium/calmodulin-dependent protein kinase type 1D, also known as CaM kinase I delta, CaM kinase ID, CaMKI-like protein kinase, CKLiK and CAMK1D, is a member of the protein kinase superfamily and CaMK subfamily. It contains one protein kinase domain. CAMK1D is broadly expressed. It is highly and mostly expressed in polymorphonuclear leukocytes (neutrophilic and eosinophilic granulocytes) while little or no expression is observed in monocytes and lymphocytes. Engineered overexpression of CAMK1D in non-tumorigenic breast epithelial cells led to increased cell proliferation, and molecular and phenotypic alterations indicative of epithelial-mesenchymal transition (EMT), including loss of cell-cell adhesions and increased cell migration and invasion. CAMK1D is a potential therapeutic target with particular relevance to clinically unfavorable basal-like tumors.