NEGR1 Polyclonal Antibody, 20ul Cell Senescence It is also known to

It is also known to be an entry co-receptor for HIV-1

Defects in HSPB1 are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

where it partially colocalizes with the nuclear lamina

This receptor is localized to the limbic areas of the brain

Heat shock protein HSP 90-alpha aids in the proper folding of specific target proteins by use of an ATPase activity that is modulated by co-chaperones

NEGR1 Polyclonal Antibody, 20ul Cell Senescence It is also known toNEGR1 is a Protein Coding gene. Diseases associated with NEGR1 include podoconiosis. Among its related pathways are Cell adhesion molecules (CAMs). An important paralog of this gene is LSAMP. May be involved in cell adhesion. May function as a trans neural growth promoting factor in regenerative axon sprouting in the mammalian brain.