Search results for receptor tyrosine kinase
SRC Proto-Oncogene, Non-Receptor Tyrosine Kinase (SRC) Antibody, Abbexa, abx126647
SRC Antibody is a Rabbit Polyclonal against SRC.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
IHC
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
SRC Proto-Oncogene, Non-Receptor Tyrosine Kinase (SRC) Antibody, Abbexa, abx033642
The gene for SRC is highly similar to the v-src gene of Rous sarcoma virus. This proto-oncogene may play a role in the regulation of embryonic development and cell growth. SRC, the protein encoded by this gene, is a tyrosine-protein kinase whose activity can be inhibited by phosphorylation by c-SRC kinase. Mutations in SRC could be involved in the malignant progression of colon cancer.
Host
Rabbit
Reactivity
Human, Mouse
Applications
ELISA, WB, IHC, IF/ICC
Conjugation
Unconjugated
Receptor Tyrosine Kinase Like Orphan Receptor 1 (ROR1) Antibody, Abbexa, abx431844
ROR1 Antibody is a Goat Polyclonal antibody against ROR1.
Host
Goat
Reactivity
Human
Applications
P-ELISA, IHC
Conjugation
Unconjugated
SRC Proto-Oncogene, Non-Receptor Tyrosine Kinase (SRC) Antibody, Abbexa, abx116642
V-Src Sarcoma (Schmidt-Ruppin A-2) Viral Oncogene Homolog (Avian) Antibody is a Rabbit Polyclonal antibody against V-Src Sarcoma (Schmidt-Ruppin A-2) Viral Oncogene Homolog (Avian).
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB, IHC, IF/ICC, IP
Conjugation
Unconjugated
Human BMX Non-Receptor Tyrosine Kinase (BMX) ELISA Kit, Abbexa, abx251507
Human BMX Non-Receptor Tyrosine Kinase (BMX) ELISA Kit is an ELISA Kit for the in vitro quantitative measurement of Human Cytoplasmic tyrosine-protein kinase BMX concentrations in tissue homogenates, cell lysates and other biological fluids.
Host
Reactivity
Human
Applications
ELISA
Conjugation
Human Muscle Skeletal Receptor Tyrosine Kinase (MUSK) ELISA Kit, Abbexa, abx250353
Human Muscle, skeletal receptor tyrosine-protein kinase ELISA Kit is an ELISA kit against Human Muscle, skeletal receptor tyrosine-protein kinase (MUSK).
Host
Reactivity
Human
Applications
ELISA
Conjugation
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
SRC Proto-Oncogene, Non-Receptor Tyrosine Kinase (SRC) Antibody, Abbexa, abx034619
This gene is highly similar to the v-src gene of Rous sarcoma virus. This proto-oncogene may play a role in the regulation of embryonic development and cell growth. The protein encoded by this gene is a tyrosine-protein kinase whose activity can be inhibited by phosphorylation by c-SRC kinase. Mutations in this gene could be involved in the malignant progression of colon cancer. Two transcript variants encoding the same protein have been found for this gene.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB, IHC, IF/ICC, FCM
Conjugation
Unconjugated
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