qPCR 96 Well Plate Optical Sealing Membrane (Non-Sticky adhesive, same with ABI 4311971)
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Catalog numberMB-QSM
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Price:
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Size2 Box
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Packing Box10 membranes/bag, 10 bags/box
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DescriptionAssociated membrane protein types are lipopolysaccharide selective barriers. Biological membranes include cell membranes, outer coverings of cells or organelles that allow passage of certain proteins and nuclear membranes, which cover a cell nucleus; and tissue membranes, such as mucosae and serosae. , A microtiter plate (spelled Microtiter is a registered trade name in the United States) or microplate or micro well plate or multiwell, is a flat plate with multiple "wells" used as small test tubes. The microplate has become a standard tool in analytical research and clinical diagnostic testing laboratories. A very common usage is in the enzyme-linked immunosorbent assay (ELISA), the basis of most modern medical diagnostic testing in humans and animals. A microplate typically has 6, 24, 96, 384 or 1536 sample wells arranged in a 23 rectangular matrix. Some microplates have even been manufactured with 3456 or 9600 wells, and an "array tape" product has been developed that provides a continuous strip of microplates embossed on a flexible plastic tape.
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Gene target
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Gene symbolABI1, ABI2
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Short nameqPCR 96 Optical Sealing (Non-Sticky adhesive, same with ABI 4311971)
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Alternative nameQuantitative real-time PCR test kit 96 Well Plate Optical Sealing Membrane (Non-Sticky adhesive, same including ABI 4311971)
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Gene info
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Identity
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Gene
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Long gene nameabl interactor 1
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Synonyms gene
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Synonyms gene name
- spectrin SH3 domain binding protein 1
- abl-interactor 1
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Synonyms
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GenBank acession
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Locus
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Discovery year1999-05-17
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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VEGA ID
Gene info
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Identity
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Gene
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Long gene nameabl interactor 2
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Synonyms gene name
- abl-interactor 2
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Synonyms
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GenBank acession
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Locus
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Discovery year2004-03-11
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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Classification
- SCAR/WAVE complex
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VEGA ID
MeSH Data
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Name
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ConceptScope note: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
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Tree numbers
- E05.393.620.500
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Qualifiersethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data