IRPL1 Polyclonal Antibody, 20ul Liquid Handling ＆Storage Mutations in CYB5R3 cause methemoglobinemias

Mutations in CYB5R3 cause methemoglobinemias

there is an extracellular spacer domain and a long

It is thought to function in neurite outgrowth and process elongation during neuronal differentiation

The protein may function as a growth or differentiation factor receptor

the homolog of CASP12 mediates apoptosis in response to endoplasmic reticulum stress

IRPL1 Polyclonal Antibody, 20ul Liquid Handling ＆Storage Mutations in CYB5R3 cause methemoglobinemiasThe protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins. It is most closely related to interleukin 1 receptor accessory protein like 2 (IL1RAPL2). This gene and IL1RAPL2 are located at a region on chromosome X that is associated with X linked non syndromic mental retardation. Deletions and mutations in this gene were found in patients with mental retardation. This gene is