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MCLN2 Rabbit Polyclonal Antibody, 100ul Enzyme-Linked Immunosorbent Assay (ELISA) Mutations in this gene have

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SEK123.75 SEK162.75

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MCLN2 Rabbit Polyclonal Antibody, 100ul Enzyme-Linked Immunosorbent Assay (ELISA) Mutations in this gene haveMucolipins constitute a family of cation channel proteins with homology to the transient receptor potential superfamily. In mammals the mucolipin family includes 3 members MCOLN1 (MIM 605248) MCOLN2 and MCOLN3 (MIM 607400) that exhibit a common 6 membrane spanning topology. Homologs of mammalian mucolipins exist in Drosophila and C. elegans. Mutations in the human MCOLN1 gene cause mucolipodosis IV (MIM 262650) (Karacsonyi et al. 2007

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Description

Mutations in this gene have been linked to cryptogenic cirrhosis

|The C-terminus of p100 might be involved in cytoplasmic retention| inhibition of DNA-binding by p52 homodimers| and/or transcription activation

MAP3K7 and TAB1

ARID1B (AT-rich interaction domain 1B) encodes an AT-rich DNA interacting domain-containing protein

This ARF product functions as a stabilizer of the tumor suppressor protein p53 as it can interact with

MCLN2 Rabbit Polyclonal Antibody, 100ul Enzyme-Linked Immunosorbent Assay (ELISA) Mutations in this gene haveMucolipins constitute a family of cation channel proteins with homology to the transient receptor potential superfamily. In mammals the mucolipin family includes 3 members MCOLN1 (MIM 605248) MCOLN2 and MCOLN3 (MIM 607400) that exhibit a common 6 membrane spanning topology. Homologs of mammalian mucolipins exist in Drosophila and C. elegans. Mutations in the human MCOLN1 gene cause mucolipodosis IV (MIM 262650) (Karacsonyi et al. 2007

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