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NIPA2 Rabbit Polyclonal Antibody, 100ul Vector Construction The protein encoded by APBA3

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NIPA2 Rabbit Polyclonal Antibody, 100ul Vector Construction The protein encoded by APBA3This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3 7 and 21.

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Description

The protein encoded by APBA3 (amyloid beta precursor protein binding family A member 3) is a member of the X11 protein family

NIK and IKKα (IKK1) regulate the phosphorylation and processing of NF-κB2 (p100) to produce p52

sequence-specific DNA binding and RNA polymerase II transcription coactivator activity

Alterations of this gene| including point mutations| insertions and deletions| cause factor IX deficiency| which is a recessive X-linked disorder| also called hemophilia B or Christmas disease

NIPA2 Rabbit Polyclonal Antibody, 100ul Vector Construction The protein encoded by APBA3This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3 7 and 21.

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