ASPC1 Rabbit Polyclonal Antibody, 20ul Antisense Oligonucleotides with the central portion containing

with the central portion containing the catalytic site

Mutations in this gene cause autosomal recessive nonsyndromic deafness| type 18B

MLLT10 encodes a transcription factor (myeloid/lymphoid or mixed-lineage leukemia

The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities

and activated macrophages but is inactive on peripheral blood lymphocytes and neutrophils

ASPC1 Rabbit Polyclonal Antibody, 20ul Antisense Oligonucleotides with the central portion containingThe protein encoded by this gene contains a UBX domain and interacts with glucose transporter type 4 (GLUT4). This protein is a tether, which sequesters the GLUT4 in intracellular vesicles in muscle and fat cells in the absence of insulin, and redistributes the GLUT4 to the plasma membrane within minutes of insulin stimulation. Translocation t(X; 17)(p11; q25) of this gene with transcription factor TFE3 gene results in a ASPSCR1 TFE3 fusion protein in