Rabbit Secondary Antibodies
ABclonal Technology SMG1 Rabbit mAb
This gene encodes a protein involved in nonsense-mediated mRNA decay (NMD) as part of the mRNA surveillance complex The protein has kinase activity and is thought to function in NMD by phosphorylating the regulator of nonsense transcripts 1 protein Alternatively spliced transcript variants have been described but their full-length nature has yet to be determined
Cayman Chemical ProsteInCTerm RabbIt Mon 100uL
A flavonoid glycoside with diverse biological activities inhibits CAVII (Ki 4 6 nM) scavenges DPPH and superoxide radicals (IC50s 12 8 and 42 UM respectively) cytotoxic to Jurkat HepG2 and COLO 205 cells (IC50s 11 6 14 3 and 55 4 UM respectively) reduces TPA-induced ear edema (ID50 0 357 mg/ear) decreases triglyceride accumulation in the liver and skeletal muscle in high-fat diet-fed KKAy diabetic mice at 100 mg/kg
Cayman Chemical Akt1CTerm RabbIt Monclon 100uL
A cytosine derivative originally found to be an inhibitor of TET1 and TET2 (IC50s 33 and 73 UM respectively in cell-free assays) however it was found that the TET inhibitory activity was due to residual copper in the preparation copper-containing Bobcat 339 reduces DNA 5-hmC levels in HT22 hippocampal neurons at 10 UM but copper-free preparations do not reduce DNA 5-hmC levels in Hep3B cells at 50 UM
ABclonal Technology ALK Rabbit mAb
This gene encodes a receptor tyrosine kinase which belongs to the insulin receptor superfamily This protein comprises an extracellular domain an hydrophobic stretch corresponding to a single pass transmembrane region and an intracellular kinase domain It plays an important role in the development of the brain and exerts its effects on specific neurons in the nervous system This gene has been found to be rearranged mutated or amplified in a series of tumours including anaplastic large cell lymphomas neuroblastoma and non-small cell lung cancer The chromosomal rearrangements are the most common genetic alterations in this gene which result in creation of multiple fusion genes in tumourigenesis including ALK (chromosome 2) EML4 (chromosome 2) ALK RANBP2 (chromosome 2) ALK ATIC (chromosome 2) ALK TFG (chromosome 3) ALK NPM1 (chromosome 5) ALK SQSTM1 (chromosome 5) ALK KIF5B (chromosome 10) ALK CLTC (chromosome 17) ALK TPM4 (chromosome 19) and ALK MSN (chromosome X)
Immunology Consultants anti-Horse Whole Serum Antibody (Rabbit) - Antiserum
This rabbit antiserum against horse whole serum provides broad, multi‑epitope recognition of equine serum proteins. Ideal for ELISA, immunodiffusion, and veterinary diagnostic development, it delivers consistent performance across diverse assay formats. Produced by Immunology Consultants, this 1 ml reagent supports robust detection of horse serum components in both purified and complex samples
American Research Products Inc Rabbit Bone Alkaline Phosphata
Rabbit Bone Alkaline Phosphatase (BALP) ELISA Kit from CUSABIO Detection Range 0 156 mIU/mL-10 mIU/mL Sensitivity 0 039 mIU/mL Sample serum plasma Method Sandwich
Jackson Immuno Research Labs AffiniPure Rabbit Anti-Horse IgG (H+L)
AffiniPure Rabbit Anti-Horse IgG (H+L)
Jackson Immuno Research Labs Rhodamine (TRITC)-AffiniPure Rabbit Anti-Horse IgG (H+L)
Rhodamine (TRITC)-AffiniPure Rabbit Anti-Horse IgG (H+L)
Cayman Chemical RabbIt ntI-T7 IgGSureLIght 1ea
Rabbit Anti-T7 IgG conjugated to SureLight™ R-PEAntibody: Anti-T7 tag (MASMTGGQQMG) IgGUses: Flow cytometry, fluorescence-activated cell sorting, and protein microarrays
ABclonal Technology 488 Rabbit anti-Human IgE
IgE is the class of antibodies produced in the lungs skin and mucous membranes It may protect against parasite invasion but it is a major factor in allergic reactions The antigen-specific IgE interacts with mast cells and eosinophils triggers the release of histamine leukotrienes and other substances that lead to the itching sneezing and congestion of allergies - and the life threatening respiratory distress of asthma and anaphylactic shock
ABclonal Technology 647 Rabbit anti-Human CD142
This gene encodes coagulation factor III a cell surface glycoprotein essential for initiating blood coagulation It acts as a high-affinity receptor for factor VII forming a complex that triggers protease cascades via limited proteolysis Unlike other coagulation cofactors factor III is fully functional when expressed on cell surfaces such as on monocytes It has extracellular transmembrane and cytoplasmic domains Platelets and monocytes express this factor during procoagulatory and proinflammatory responses Factor III is implicated in HIV-related coagulopathy and is associated with COVID-19 severity and mortality Notably congenital deficiency of this protein has not been observed Multiple transcript variants exist due to alternative splicing
ABclonal Technology PE Rabbit anti-Human IgA1 mAb
Ig alpha is the major immunoglobulin class in body secretions It may serve both to defend against local infection and to prevent access of foreign antigens to the general immunologic system In normal adult serum the approximate percentage composition of IgA with respect to is subclasses is IgA1 90% and IgA2 10% In secretory IgA the subclass proportions may approach 50 50 The clinical significance of the subclasses has yet to be determined
ABclonal Technology PE Rabbit anti-Human FGFR3 mAb
This gene encodes a member of the fibroblast growth factor receptor (FGFR) family with its amino acid sequence being highly conserved between members and among divergent species FGFR family members differ from one another in their ligand affinities and tissue distribution A full-length representative protein would consist of an extracellular region composed of three immunoglobulin-like domains a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain The extracellular portion of the protein interacts with fibroblast growth factors setting in motion a cascade of downstream signals ultimately influencing mitogenesis and differentiation This particular family member binds acidic and basic fibroblast growth hormone and plays a role in bone development and maintenance Mutations in this gene lead to craniosynostosis and multiple types of skeletal dysplasia