Search results for receptor for

IL9 Receptor antibody, Genetex, GTX66479

TRH Receptor antibody, Genetex, GTX71137

TSH receptor antibody, Genetex, GTX71175

Glycine Receptor antibody, Genetex, GTX82665

LDL Receptor antibody, Genetex, GTX85109

Receptor Tyrosine Kinase Like Orphan Receptor 1 (ROR1) Antibody, Abbexa, abx431844

ROR1 Antibody is a Goat Polyclonal antibody against ROR1.

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).

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 2 (ROR2) Antibody, Abbexa, abx128158

Receptor Tyrosine Kinase Like Orphan Receptor 2 Antibody is a Rabbit Polyclonal against Receptor Tyrosine Kinase Like Orphan Receptor 2.

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody, Abbexa, abx033602

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.