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DYRL1 Rabbit Polyclonal Antibody, 50ul Protein Analysis Mutations in TUBA1A cause lissencephaly
DYRL1 Rabbit Polyclonal Antibody, 50ul Protein Analysis Mutations in TUBA1A cause lissencephaly
DYRL1 Rabbit Polyclonal Antibody, 50ul Protein Analysis Mutations in TUBA1A cause lissencephaly
DYRL1 Rabbit Polyclonal Antibody, 50ul Protein Analysis Mutations in TUBA1A cause lissencephaly

DYRL1 Rabbit Polyclonal Antibody, 50ul Protein Analysis Mutations in TUBA1A cause lissencephaly

SKU: 98481898312

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DYRL1 Rabbit Polyclonal Antibody, 50ul Protein Analysis Mutations in TUBA1A cause lissencephaly

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Description

Mutations in TUBA1A cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly

The encoded protein contains a single immunoglobulin (Ig) domain and is a receptor that relays inhibitory signals to suppress the immune response

This gene encodes a member of the proteasome B-type family| also known as the T1B family| that is a 20S core beta subunit

KIT encodes the human homolog of the proto-oncogene c-kit

Sequence polymorphisms in TFAM are associated with Alzheimer's and Parkinson's diseases

DYRL1 Rabbit Polyclonal Antibody, 50ul Protein Analysis Mutations in TUBA1A cause lissencephaly

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