Search results for receptor tyrosine kinase

Erb-B2 Receptor Tyrosine Kinase 4 (ERBB4) Antibody, Abbexa, abx326738

ERBB4 Antibody is a Rabbit Polyclonal against ERBB4.

Erb-B2 Receptor Tyrosine Kinase 2 (ERBB2) Antibody, Abbexa, abx159489

ERBB2 Antibody is a Mouse Monoclonal against ERBB2.

Neurotrophic Receptor Tyrosine Kinase 1 (NTRK1) Antibody (HRP), Abbexa, abx335952

NTRK1 Antibody (HRP) is a Rabbit Polyclonal against NTRK1.

Discoidin Domain Receptor Tyrosine Kinase 2 (DDR2) Antibody, Abbexa, abx318254

DDR2 Antibody is a Rabbit Polyclonal against DDR2.

Angiogenesis Receptor Tyrosine Kinase Antibody Sampler Kit#78451, Cell Signaling Technology (CST), 78451

Receptor Tyrosine Kinase Like Orphan Receptor 1 (ROR1) Antibody, Abbexa, abx174350

This product is currently in development. The lead time for this product may be several months. Please contact us at [email protected] for an updated lead time before purchasing this product. Receptor Tyrosine Kinase Like Orphan Receptor 1 (ROR1) Antibody is a Mouse Monoclonal antibody against Receptor Tyrosine Kinase Like Orphan Receptor 1 (ROR1).

SRC Proto-Oncogene, Non-Receptor Tyrosine Kinase (SRC) Antibody, Abbexa, abx328962

SRC Antibody is a Rabbit Polyclonal against SRC.

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody, Abbexa, abx033604

ROR2 is a tyrosine-protein kinase receptor which may be involved in the early formation of the chondrocytes. It seems to be required for cartilage and growth plate development. This Type I membrane protein is expressed at high levels during early embryonic development. The expression levels drop strongly around day 16 and there are only very low levels in adult tissues. Defects in ROR2 are a cause of brachydactyly type B1 (BDB1). BDB1 is an autosomal dominant skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In BDB1 the middle phalanges are short but in addition the terminal phalanges are rudimentary or absent. Both fingers and toes are affected. The thumbs and big toes are usually deformed. Defects in ROR2 are a cause of recessive Robinow syndrome (RRS). RRS is an autosomal disorder characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly and a dysmorphic facial appearance. The protein contains 1 frizzled (FZ) domain, 1 immunoglobulin-like C2-type domain, and 1 kringle domain.

Receptor Tyrosine Kinase Like Orphan Receptor 1 (ROR1) Antibody, Abbexa, abx449254

ROR1 Antibody is a Rabbit Polyclonal Antibody against ROR1.

SRC Proto-Oncogene, Non-Receptor Tyrosine Kinase (SRC) Antibody, Abbexa, abx329483

SRC Antibody is a Rabbit Polyclonal against SRC.