Search results for ROR2 antibody

Tyrosine-Protein Kinase Transmembrane Receptor ROR2 (ROR2) Antibody, Abbexa, abx421049
Tyrosine-Protein Kinase Transmembrane Receptor ROR2 (ROR2) Antibody is a Mouse Monoclonal antibody for the detection of Tyrosine-Protein Kinase Transmembrane Receptor ROR2 (ROR2) in Human, Monkey, Mouse samples.
Host
Mouse
Reactivity
Human, Monkey, Mouse
Applications
ELISA, FCM
Conjugation
Unconjugated

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.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB, IHC
Conjugation
Unconjugated

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.
Host
Rabbit
Reactivity
Human
Applications
WB, IHC, IF/ICC
Conjugation
Unconjugated

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.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB, IHC, FCM
Conjugation
Unconjugated

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody, Abbexa, abx334125
ROR2 Antibody is a Rabbit Polyclonal against ROR2.
Host
Rabbit
Reactivity
Human
Applications
ELISA, IHC, IF/ICC
Conjugation
Unconjugated

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody, Abbexa, abx146445
ROR2 Antibody is a Rabbit Polyclonal against ROR2.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB, IHC
Conjugation
Unconjugated

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody, Abbexa, abx033603
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.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB, IHC
Conjugation
Unconjugated

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody, Abbexa, abx328028
ROR2 Antibody is a Rabbit Polyclonal against ROR2.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB
Conjugation
Unconjugated

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody, Abbexa, abx004297
ROR2 Antibody is a Rabbit Polyclonal antibody against ROR2. The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
WB
Conjugation
Unconjugated

Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) Antibody (Biotin), Abbexa, abx338154
ROR2 Antibody (Biotin) is a Rabbit Polyclonal against ROR2.
Host
Rabbit
Reactivity
Human
Applications
ELISA
Conjugation
Biotin
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