Search results for TSPAN7 antibody

TSPAN7 antibody, Genetex, GTX34283

TSPAN7 antibody [B2D], Genetex, GTX00532

TSPAN7 Antibody (YA7992), MedChemexpress, HY-P88308

TSPAN7 Antibody (YA7992) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targating to TSPAN7.

Tetraspanin-7 (TSPAN7) Antibody, Abbexa, abx004911

TSPAN7 Antibody is a Rabbit Polyclonal antibody against TSPAN7. The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. This gene is associated with X-linked mental retardation and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy.

Tetraspanin-7 (TSPAN7) Antibody, Abbexa, abx239066

TSPAN7 Antibody is a Rabbit Polyclonal against TSPAN7.

Tetraspanin-7 (TSPAN7) Antibody, Abbexa, abx110260

Tetraspanin-7 Antibody is a Rabbit Polyclonal antibody against Tetraspanin-7.

TSPAN7 antibody [B2D] (FITC), Genetex, GTX00532-06

TSPAN7 antibody [B2D] (APC), Genetex, GTX00532-07

TSPAN7 antibody [B2D] (PE), Genetex, GTX00532-08

Tetraspanin-7 (TSPAN7) Antibody, Abbexa, abx032328

TSPAN7 is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. This gene is associated with X-linked mental retardation and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy.