ELISA Substrates and Reagents
Abcam TMB ELISA Substrate (Slower Kinetic Rate), 100ML
Abcam's TMB ELISA Substrate (Slower Kinetic Rate) detects horseradish peroxidase (HRP) activity and contains 3,3',5,5'-tetramethylbenzidine in a mildly acidic buffer.
The product is subject to the following: Abcam Restricted Use Statement
Surmodics Inc TMB Double Slow One Component HRP Microwell Substrate, 1L
BioFX™ TMB Double Slow Kinetic One Component HRP Microwell Substrate is a low-kinetic range substrate for ELISA applications.
ABclonal Technology PE anti-h CD235a/Glycophorin A
Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups In addition to the M or N and S or s antigens that commonly occur in all populations about 40 related variant phenotypes have been identified These variants include all the variants of the Miltenberger complex and several isoforms of Sta as well as Dantu Sat He Mg and deletion variants Ena S-s-U- and Mk Most of the variants are the result of gene recombinations between GYPA and GYPB
Bioss JNK - Thr-183/Tyr-185 Phospho
JNK (Thr-183/Tyr-185) Primary Antibody Unconjugated Host Species Mouse Target Species Human Mouse Rat Clonality Monoclonal Applications WB M268Concentration Size 100 ul Storage Buffer PBS 1 mg/ml BSA 0 05% NaN3 and 50% glycerol
ABclonal Technology Phospho-Filamin A-S2152 Rabbit pAb
The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.
ABclonal Technology Phospho-SHP2-Y542 Rabbit pAb
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia.
ABclonal Technology Phospho-ErbB3/HER3-Y1328 Rabbit pAb
This gene encodes a member of the epidermal growth factor receptor (EGFR) family, a membrane-bound protein that binds neuregulin but lacks an active kinase domain. It does not directly convey signals but forms heterodimers with other EGFR family members that have kinase activity. Heterodimerization activates pathways leading to cell proliferation or differentiation. Amplification or overexpression of this gene is found in cancers such as prostate, bladder, and breast tumors. Alternative splicing produces isoforms, including one that lacks the intermembrane region and is secreted to modulate the membrane-bound form’s activity. Other splice variants have been reported but are not fully characterized.
Surmodics Inc TMB Super Slow One Component HRP Microwell Substrate, 1L
The BioFX™ one component 3,3’,5,5’-tetramethylbenzidine (TMB) substrate is supplied in a ready-to-use solution. Peroxidase reacts with the TMB substrate solution to produce a soluble blue reaction product that can be read at 370 nm or 620-650 nm for ELISA applications. Stop solutions can be added to prevent further color development and reading the absorbance values at the desired wavelengths.
ABclonal Technology Phospho-BRD4-S1070 Rabbit pAb
The protein encoded by this gene is homologous to the murine protein MCAP, which associates with chromosomes during mitosis, and to the human RING3 protein, a serine/threonine kinase. Each of these proteins contains two bromodomains, a conserved sequence motif which may be involved in chromatin targeting. This gene has been implicated as the chromosome 19 target of translocation t(15,19)(q13,p13.1), which defines an upper respiratory tract carcinoma in young people. Two alternatively spliced transcript variants have been described.
ABclonal Technology 594 anti-h CD235a
Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups In addition to the M or N and S or s antigens that commonly occur in all populations about 40 related variant phenotypes have been identified These variants include all the variants of the Miltenberger complex and several isoforms of Sta as well as Dantu Sat He Mg and deletion variants Ena S-s-U- and Mk Most of the variants are the result of gene recombinations between GYPA and GYPB
ABclonal Technology 594 anti-h CD235a
Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups In addition to the M or N and S or s antigens that commonly occur in all populations about 40 related variant phenotypes have been identified These variants include all the variants of the Miltenberger complex and several isoforms of Sta as well as Dantu Sat He Mg and deletion variants Ena S-s-U- and Mk Most of the variants are the result of gene recombinations between GYPA and GYPB
ABclonal Technology 594 anti-h CD235a
Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups In addition to the M or N and S or s antigens that commonly occur in all populations about 40 related variant phenotypes have been identified These variants include all the variants of the Miltenberger complex and several isoforms of Sta as well as Dantu Sat He Mg and deletion variants Ena S-s-U- and Mk Most of the variants are the result of gene recombinations between GYPA and GYPB