Antibody and Dye Based Assays
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Filtered Search Results
Promega ADCC Reporter Bioassay, Target (WIL2-S)
Recommended for use as a control with all Fc Effector Bioassay Core Kits. ADCC Reporter Bioassay provides a biologically relevant and specific mechanism-of-action-based measure of ADCC without the complex workflow and variability inherent in primary cell-based assays.
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Promega ADCC Reporter Bioassay, Target (Raji)
Recommended for use as a control with all Fc Effector Bioassay Core Kits. ADCC Reporter Bioassay provides a biologically relevant and specific mechanism-of-action-based measure of ADCC without the complex workflow and variability inherent in primary cell-based assays.
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Promega ADCC Reporter Bioassay, Complete (Raji)
Provides a biologically relevant and specific mechanism-of-action-based measure of ADCC without the complex workflow and variability inherent in primary cell-based assays. The bioassay also can be used to quantify effects of antibody glycosylation on Fc effector function.
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Thermo Scientific™ LanthaScreen™ Tb-labeled Anti-Goat Ab
This product is ideally suited for use during assay development when evaluating multiple primary goat antibodies, or when it is not possible to directly terbium label a primary antibody.
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| Shipping Condition | Dry Ice |
|---|---|
| Excitation/Emission | 340/490, 520 |
| Content And Storage | Terbium-labeled anti-Goat antibody in HEPES buffered saline. Store at -20°C. |
| Reactivity | Goat |
| Conjugate | Lanthanide Chelates, Terbium (Tb) |
| Readout | End Point |
| Product Line | LanthaScreen |
Romer Labs AgraStrip Gluten G12 test kits, 10 tests, 11-12 min assay time, qualitative result, gluten detection, antibody G12 monoclonal
AgraStrip Gluten G12 test kits, 10 tests, 11-12 min assay time, qualitative result, gluten detection, antibody G12 monoclonal
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Abcam PE / R-Phycoerythrin Conjugation Kit - Lightning-Link, 600UG
The Abcam PE/R-Phycoerythrin Conjugation Kit (ab102918) offers several standout features: -Rapid Conjugation: achieve PE/R-Phycoerythrin labeling in under 4 hours with just 30 seconds of hands-on time. -High Efficiency: ensures 100% antibody recovery, preserving the integrity and value of your antibodies. -Versatility: suitable for conjugating antibodies, proteins, and peptides, and the labeled antibodies can be used immediately in applications such as Western Blotting (WB), ELISA, and Immunohistochemistry (IHC) without further purification. - Confidence: cited in over 50 publications
The product is subject to the following: Abcam Restricted Use Statement
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Abcam Phalloidin-iFluor 488 Reagent
Phalloidin-iFluor 488 Reagent
The product is subject to the following: Abcam Restricted Use Statement
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Abcam DAPI Staining Solution
DAPI Staining Solution
The product is subject to the following: Abcam Restricted Use Statement
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US Biomax Inc HEAD & NECK CANCER TISSUE ARRA
Head & Neck cancer tissue array with unmatched normal adjacent tissues
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Biotium Desmocollin-2/3 (7G6), CF488A conjugate, 0.1mg/mL
Desmosomes are intercellular adhering junctions that represent cell surface attachment sites for intermediate filament. The desmosome is subdivided into two regions. The plaque region lies adjacent to the plasma, and is believed to contain molecules that attach the intermediate filament cytoskeleton to the desmosome. The core region is composed of transmembrane glycoproteins that are thought to mediate cell-cell adhesion. Desmogleins and desmocollins are the main desmosomal transmembrane proteins. These desmosomal glycoproteins belong to the members of the cadherin family of adhesion molecules. Three different isoforms of both desmogleins and desmocollins have been identified, named as desmoglein 1-3 and desmocollins. Desmosomal cadherins showed differentiation-specific expression in the human epidermis, although the functional significance of this differential expression is not fully understood. Desmocollin-1 can be found in the upper layers. The expression of desmocollin-2
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Biotium CD43(DF-T1), CF488A conjugate, 0.1mg/mL
This antibody recognizes a cell surface glycoprotein of 95/115/135 kDa (depending upon the extent of glycosylation), identified as CD43 . Epitope of MAb Bra7G is clearly different from that of MAb DF-T1, called b as opposed to a for DF-T1. 70-90% of T-cell lymphomas and from 22-37% of B-cell lymphomas express CD43. No reactivity has been observed with reactive B-cells. So a B-lineage population that co-expresses CD43 is highly likely to be a malignant lymphoma, especially a low-grade lymphoma, rather than a reactive B-cell population. When CD43 antibody is used in combination with anti-CD20, effective immunophenotyping of the lymphomas in formalin-fixed tissues can be obtained. Co-staining of a lymphoid infiltrate with anti-CD20 and anti-CD43 argues against a reactive process and favors a diagnosis of lymphoma.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note
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Biotium HCG-beta(HCGb/54), CF488A conjugate, 0.1mg/mL
This MAb reacts with a protein of 22 kDa, identified as β sub-unit of HCG. It does not cross react with the α sub-unit. HCG is a glycoprotein, which is secreted in large quantities by normal trophoblasts. It is present only in trace amounts in non-pregnant urine and sera but rises sharply during pregnancy. HCG is composed of two non-identical, non-covalently linked polypeptide chains designated as the alpha and beta subunits. The alpha subunit is identical to that of thyroid stimulating hormone (TSH), follicle stimulating hormone (FSH), and luteinizing hormone (LH). hCG MAb detects cells and tumors of trophoblastic origin such as choriocarcinoma. Large cell carcinoma and adenocarcinoma of the lung demonstrate anti-hCG positivity in 90% and 60% of cases respectively. 20% of lung squamous cell carcinomas are positive. hCG expression by non-trophoblastic tumors may indicate aggressive behavior.Primary antibodies are available purified, or with a selection of fluoresce
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Biotium CD43(DF-T1), CF488A conjugate, 0.1mg/mL
This antibody recognizes a cell surface glycoprotein of 95/115/135 kDa (depending upon the extent of glycosylation), identified as CD43 . Epitope of MAb Bra7G is clearly different from that of MAb DF-T1, called b as opposed to a for DF-T1. 70-90% of T-cell lymphomas and from 22-37% of B-cell lymphomas express CD43. No reactivity has been observed with reactive B-cells. So a B-lineage population that co-expresses CD43 is highly likely to be a malignant lymphoma, especially a low-grade lymphoma, rather than a reactive B-cell population. When CD43 antibody is used in combination with anti-CD20, effective immunophenotyping of the lymphomas in formalin-fixed tissues can be obtained. Co-staining of a lymphoid infiltrate with anti-CD20 and anti-CD43 argues against a reactive process and favors a diagnosis of lymphoma.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note
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Abcam Phalloidin-iFluor 647 Reagent
Phalloidin-iFluor 647 Reagent
The product is subject to the following: Abcam Restricted Use Statement
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Biotium Cyclin D1(DCS-6), CF488A conjugate, 0.1mg/mL
Recognizes a protein of 36 kDa, identified as cyclin D1. Cyclin D1, one of the key cell cycle regulators, is a putative proto-oncogene overexpressed in a wide variety of human neoplasms. This antibody neutralizes the activity of cyclin D1 in vivo. About 60% of mantle cell lymphomas (MCL) contain a t(11; 14)(q13; q32) translocation resulting in over-expression of cyclin D1. This antibody is useful in identifying mantle cell lymphomas (cyclin D1 positive) from CLL/SLL and follicular lymphomas (cyclin D1 negative). About 40% of breast carcinomas are positive for Cyclin D1. Occasionally, hairy cell leukemia and plasma cell myeloma weakly express Cyclin D1.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 fluorescenc
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