Primary Antibody Matched Pairs
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Filtered Search Results
Sino Biological Human IL-5 Matched ELISA Antibody Pair Set 15 Plates
The Human IL-5/IL5 / Interleukin 5 ELISA Pair Set is for the quantitative determination of Human IL-5/IL5 / Interleukin 5.The Sino Biological ELISA Pair Set is a solid phase sandwich ELISA (Enzyme-Linked Immunosorbent Assay). It utilizes a monoclonal antibody specific for Human IL-5/IL5 / Interleukin 5 coated on a 96-well plate. Standards and samples are added to the wells, and any Human IL-5/IL5 / Interleukin 5 present binds to the immobilized antibody. The wells are washed and a horseradish peroxidase conjugated rabbit anti-Human IL-5/IL5 / Interleukin 5 monoclonal antibody is then added, producing an antibody-antigen-antibody "sandwich". The wells are again washed and TMB substrate solution is loaded, which produces color in proportion to the amount of Human IL-5/IL5 / Interleukin 5 present in the sample. To end the enzyme reaction, the stop solution is added and absorbances of the microwell are read at 450 nm.
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Sino Biological Human CD84 Matched ELISA Antibody Pair Set 5 Plates
The human CD84 ELISA Pair Set is for the quantitative determinationof human CD84.This ELISA Pair Set contains the basic components required for the development of sandwich ELISAs.The Sino Biological ELISA Pair Set is asolid phase sandwich ELISA (Enzyme-Linked ImmunosorbentAssay). It utilizes a monoclonal antibody specific for CD84 coatedon a 96-well plate. Standards and samples are added to the wells, and any CD84 presentbinds to the immobilized antibody. The wells are washed and a horseradish peroxidase conjugated mouse anti-CD84 monoclonal antibody is then added, producing an antibody-antigen-antibody"sandwich". The wells are again washed and TMB substrate solution is loaded,which produces color in proportion to the amount of CD84 presentin the sample. To end the enzyme reaction, the stop solution is added and absorbances of the microwell are read at 450 nm.
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Sino Biological Mouse IL-1 alpha/IL1A Matched ELISA Antibody Pair Set 15 Plates
The Mouse IL-1 alpha / IL-1F1 / IL1A ELISA Pair Set is for the quantitative determination of Mouse IL-1 alpha / IL-1F1 / IL1A.The Sino Biological ELISA Pair Set is a solid phase sandwich ELISA (Enzyme-Linked Immunosorbent Assay). It utilizes a monoclonal antibody specific for Mouse IL-1 alpha / IL-1F1 / IL1A coated on a 96-well plate. Standards and samples are added to the wells, and any Mouse IL-1 alpha / IL-1F1 / IL1A present binds to the immobilized antibody. The wells are washed and a horseradish peroxidase conjugated rabbit anti-Mouse IL-1 alpha / IL-1F1 / IL1A polyclonal antibody is then added, producing an antibody-antigen-antibody "sandwich". The wells are again washed and TMB substrate solution is loaded, which produces color in proportion to the amount of Mouse IL-1 alpha / IL-1F1 / IL1A present in the sample. To end the enzyme reaction, the stop solution is added and absorbances of the microwell are read at 450 nm.
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Sino Biological Human IL-20R alpha/IL-20RA Matched ELISA Antibody Pair Set 15 Plates
The human IL20RA / IL20R1 ELISA Pair Set is for the quantitative determination of human IL20RA / IL20R1.This ELISA Pair Set contains the basic components required for the development of sandwich ELISAs.The Sino Biological ELISA Pair Set is a solid phase sandwich ELISA (Enzyme-Linked Immunosorbent Assay). It utilizes a monoclonal antibody specific for IL20RA /IL20R1 coated on a 96-well plate. Standards and samples are added to the wells,and any IL20RA / IL20R1 present binds to the immobilized antibody. The wellsare washed and a horseradish peroxidase conjugated rabbit anti-IL20RApolyclonal antibody is then added, producing an antibody-antigen-antibody"sandwich". The wells are again washed and TMB substrate solution is loaded,which produces color in proportion to the amount of IL20RA / IL20R1 present inthe sample. To end the enzyme reaction, the stop solution is added andabsorbances of the microwell are read at 450 nm.
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Biotium MALT1 (MALT-Lymphoma Marker)(rMT1/410), CF568 conjugate, 0.1mg/mL
Mucosa associated lymphoid tissue lymphoma translocation gene 1 (MALT1) is found in extranodal low-grade B cell lymphomas. MALT1 encodes two Ig-like C2-type domains and fuses with an API2 gene, which is highly expressed in adult lymphoid tissue. The translocation of this MALT1 gene, which maps to human chromosome 18q21, and the apoptosis-inhibiting API2 gene results in an increased development of MALT lymphomas and apoptosis inhibition. Sites at which this API2-MALT1 (11;18)(q21;q21) translocation commonly occurs are within human lung and kidney tissue. MALT lymphoma expresses nuclear Bcl10, which mediates the oligomerization and activation of a MALT1 caspase-like domain. MALT1 mRNA is found in pre-B cells, mature B cells and plasma cells. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not r
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Biotium CD79b (B-Cell Marker)(rIGB/1842), CF594 conjugate, 0.1mg/mL
CD79 (also designated Ig chains, designated CD79B or B29. The B cell antigen receptor complex (BCR) is formed by the association of CD79 with a membrane immunoglobulin, such as IgM or IgD. The membrane immunoglobulins IgM and IgD achieve surface expression and antigen presentation function in response to CD79 association. The cytoplasmic tails of both CD79A and CD79B contain an ITAM (immuno-receptor tyrosine-based activation) motif, which acts to initiate the BCR signaling reactions by binding to and activating tyrosine kinases. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
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Sino Biological Recombinant Human CTLA-4 Protein (His & AVI Tag), Avi-tag Biotinylated, HPLC-verified 20 µg
A DNA sequence encoding the Human CTLA-4 (NP_005205.2) (Lys36-Phe162) was expressed with a C-terminal polyhistidine tag followed by an AVI tag. The expressed protein was biotinylated in vivo by the Biotin-Protein ligase (BirA enzyme) which is co-expressed.
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Cayman Chemical WB 4101hydrochlorIde 250mg
An α-AR antagonist; inhibits norepinephrine-induced contraction in isolated rat vas deferens (pA2 = 9.8); inhibits carbamoylcholine-induced contractions in isolated guinea pig taenia caeci (pA2 = 8.9)
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Biolegend Alexa FluorR 647 anti-Olig2
Alexa Fluor 647 anti-Olig2 [W21023A] Isotype Rat IgG2b Reactivity Human Rat Apps ICFC ICC Size 100 g
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Biotium Cathepsin D (Tumor Marker)(CTSD/3276), CF647 conjugate, 0.1mg/mL
Cathepsin D is a ubiquitously expressed lysosomal aspartyl protease involved in the normal degradation of proteins. It is synthesized as an inactive 43 kDa preprocathepsin D that is cleaved and glycosylated to form a 46 kDa procathepsin D and then further cleaved to produce 28 kDa and 15 kDa subunits (heavy and light chains, respectively). Cathepsin D exhibits pepsin-like activity and plays a role in protein turnover and in the proteolytic activation of hormones and growth factors. Mutations in this gene play a causal role in neuronal ceroid lipofuscinosis-10 and may be involved in the pathogenesis of several other diseases, including breast cancer and possibly Alzheimer's disease. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blu
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Biotium Carboxypeptidase A1 / CPA1 (Pancreatic Cancer Marker)(CPA1/2711), CF740 conjugate, 0.1mg/mL
Carboxypeptidase A1 (CPA1) is a secreted zinc metalloprotease that is highly expressed in pancreatic tissue. It catalyzes the release of C-terminal amino acids from a variety of proteins, thereby playing a key role in protein digestion and degradation. Human pancreatic procarboxypeptidase A exists as three different active forms, two of which are carboxypeptidase A1 (CPA1) and carboxypeptidase A2 (CPA2). Abnormal levels of CPA1 are associated with pancreatic cancer, suggesting a possible role in either tumor progression or tumor suppression events. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
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Biotium CD209 / DC-SIGN (Pathogen Receptor on Dendritic Cells)(C209/2749R), CF594 conjugate, 0.1mg/mL
DC-SIGN is a transmembrane receptor that is expressed on the surface of dendritic cells and macrophages. It is involved in the innate immune system and recognizes numerous evolutionarily divergent pathogens ranging from parasites to viruses. The protein is organized into three distinct domains: an N-terminal transmembrane domain, a tandem-repeat neck domain and C-type lectin carbohydrate recognition domain. The extracellular region consisting of the C-type lectin and neck domains has a dual function as a pathogen recognition receptor and a cell adhesion receptor by binding carbohydrate ligands on the surface of microbes and endogenous cells. The neck region is important for homo-oligomerization, which allows the receptor to bind multivalent ligands with high avidity. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like C
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Biotium MMP3 (Marker of Metastasis and Rheumatoid Arthritis)(MMP3/2655), CF568 conjugate, 0.1mg/mL
The matrix metalloproteinases (MMP) are a family of peptidase enzymes responsible for the degradation of extracellular matrix components, including collagen, gelatin, fibronectin, laminin and proteoglycan. Transcription of MMP genes is differentially activated by phorbol ester, lipopolysaccharide (LPS) or staphylococcal enterotoxin B (SEB). MMP catalysis requires both calcium and zinc. MMP-3, MMP-10 and MMP-11 (also designated stromelysin-1, 2 and 3, respectively) activate procollagenase. MMP-3 activation of procollagenase can occur via two pathways. Direct activation by MMP-3 is slow and activation by MMP-3 in conjunction with tissue or plasma proteinases is rapid. MMP-10 is expressed in small intestine, and at lower levels in lung and heart. MMP-11 is specifically expressed in stromal cells of breast carcinomas and contributes to epithelial cell malignancies. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes of
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Medchemexpress LLC CRABP2 protein, mouse (His) | >95.0% | 10 UG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Recombinant mouse CRABP2 (cellular retinoic acid-binding protein 2) is supplied as a His-tagged, partially truncated fragment (P2-E138) expressed in E. coli and provided lyophilized for biochemical and ligand-binding studies.
- Expression system: E. coli.
- Tag: N-terminal 6xHis.
- Purity: >95.0% by reducing SDS-PAGE.
- Molecular weight: ~16 kDa.
- Formulation: lyophilized from PBS, pH 7.4.
- Available sizes: 5 μg, 10 μg, 50 μg, 100 μg.
- Storage: store at -20°C; aliquot and keep at -80°C for long term.
- Reconstitution: recommended ≥100 μg/mL in ddH2O.
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Human AFP ELISA Pair Set 5PP (Sino Biological)
Each vial contains 100 ng of recombinant Human AFP / alpha-fetoprotein. Reconstitute with 1 mL Dilution Buffer. After reconstitution, store at -20℃ to -80℃ in a manual defrost freezer. A seven-point standard curve using 2-fold serial dilutions in Dilution Buffer, and a high standard of 1000 pg/mL is recommended.
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