You Searched For: 5(6)-Carboxytetramethylrhodamine+succinimidyl+ester+[5(6)-TAMRA+S


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Description: CRP2BP is a 782 amino acid protein encoded by the human gene CSRP2BP. CRP2BP specifically interacts with the double LIM domain protein CRP2. The LIM domain is a conserved cysteine and histidine-containing structural module of two tandemly arranged zinc fingers. It has been identified in single or multiple copies in a variety of regulatory proteins, either in combination with defined functional domains, like homeodomains, or alone, like in the CRP family of LIM proteins. Members of the cysteine- and glycine-rich protein family (CRP1, CRP2 and CRP3) contain two zinc-binding LIM domains, LIM1 (amino-terminal) and LIM2 (carboxyl-terminal), and are implicated in diverse cellular processes linked to differentiation, growth control and pathogenesis. Although present in cytoplasm, CRP2BP is mainly a ubiquitously expressed nuclear protein, with highest expression in skeletal muscle and heart.
Catalog Number: BOSSBS-12947R-CY5
UOM: 1 * 100 µl
Supplier: Bioss


Description: 4-Hydroxybenzamide ≥98%
Catalog Number: B24222.14
UOM: 1 * 25 g
Supplier: Thermo Fisher Scientific

MSDS


Description: Ethyl-5-amino-1-phenyl-1H-pyrazole-4-carboxylate
Catalog Number: MOLE43889017-5G
UOM: 1 * 5 g
Supplier: Molekula


Description: 4-Fluorobenzamide ≥98%
Catalog Number: L06831.22
UOM: 1 * 100 g
Supplier: Thermo Fisher Scientific

Description: A gene of chromosome 6q23 encodes the 640 amino acid protein, EYA4 (eyes absent) (1). EYA is one of four members of the eyes absent family (1). A 271 amino acid domain at the carboxyl terminal is highly conserved amongst the members of the eyes absent family (1). EYA4 is expressed in the craniofacial mesenchyme, the dermamyotome, and the limb (1). The conserved region in other EYA proteins interacts with SIX, DACH, and G-proteins, which regulate transcription in early embryonic development (1,2,3,4). SIX translocates EYA1-3 to the nucleus, and G-proteins can stop this interaction (3,4). Premature stop codon mutations in EYA4 cause postlingual, progressive autosomal dominant hearing loss in humans (2). This shows that EYA4 is also vital to the mature organ of Corti (2). EYA4 may cause oculo-dento-digital syndrome, based on its expression pattern and map postion (1).
Catalog Number: BOSSBS-13126R-CY7
UOM: 1 * 100 µl
Supplier: Bioss


Description: A gene of chromosome 6q23 encodes the 640 amino acid protein, EYA4 (eyes absent) (1). EYA is one of four members of the eyes absent family (1). A 271 amino acid domain at the carboxyl terminal is highly conserved amongst the members of the eyes absent family (1). EYA4 is expressed in the craniofacial mesenchyme, the dermamyotome, and the limb (1). The conserved region in other EYA proteins interacts with SIX, DACH, and G-proteins, which regulate transcription in early embryonic development (1,2,3,4). SIX translocates EYA1-3 to the nucleus, and G-proteins can stop this interaction (3,4). Premature stop codon mutations in EYA4 cause postlingual, progressive autosomal dominant hearing loss in humans (2). This shows that EYA4 is also vital to the mature organ of Corti (2). EYA4 may cause oculo-dento-digital syndrome, based on its expression pattern and map postion (1).
Catalog Number: BOSSBS-13126R-FITC
UOM: 1 * 100 µl
Supplier: Bioss


Description: A gene of chromosome 6q23 encodes the 640 amino acid protein, EYA4 (eyes absent) (1). EYA is one of four members of the eyes absent family (1). A 271 amino acid domain at the carboxyl terminal is highly conserved amongst the members of the eyes absent family (1). EYA4 is expressed in the craniofacial mesenchyme, the dermamyotome, and the limb (1). The conserved region in other EYA proteins interacts with SIX, DACH, and G-proteins, which regulate transcription in early embryonic development (1,2,3,4). SIX translocates EYA1-3 to the nucleus, and G-proteins can stop this interaction (3,4). Premature stop codon mutations in EYA4 cause postlingual, progressive autosomal dominant hearing loss in humans (2). This shows that EYA4 is also vital to the mature organ of Corti (2). EYA4 may cause oculo-dento-digital syndrome, based on its expression pattern and map postion (1).
Catalog Number: BOSSBS-13126R-CY3
UOM: 1 * 100 µl
Supplier: Bioss


Description: Degrades bioactive fatty acid amides like oleamide, the endogenous cannabinoid, anandamide and myristic amide to their corresponding acids, thereby serving to terminate the signaling functions of these molecules. Hydrolyzes polyunsaturated substrate anandamide preferentially as compared to monounsaturated substrates.
Catalog Number: BOSSBS-5104R-CY5
UOM: 1 * 100 µl
Supplier: Bioss


Description: 2-Fluorobenzamide 98%
Catalog Number: APOSPC3472-25G
UOM: 1 * 25 g
Supplier: Apollo Scientific


Description: 4-Chlorobenzamide ≥98%
Catalog Number: A13809.30
UOM: 1 * 250 g
Supplier: Thermo Fisher Scientific

Description: Degrades bioactive fatty acid amides like oleamide, the endogenous cannabinoid, anandamide and myristic amide to their corresponding acids, thereby serving to terminate the signaling functions of these molecules. Hydrolyzes polyunsaturated substrate anandamide preferentially as compared to monounsaturated substrates.
Catalog Number: BOSSBS-5104R-A350
UOM: 1 * 100 µl
Supplier: Bioss


Description: 2-Ethoxybenzamide ≥97%
Catalog Number: B25455.22
UOM: 1 * 100 g
Supplier: Thermo Fisher Scientific

Description: Anthranilamide 99+%
Catalog Number: ACRO104901000
UOM: 1 * 100 g
Supplier: Thermo Fisher Scientific

MSDS


Description: Anti-QPRT Mouse Polyclonal Antibody
Catalog Number: USBI132149
UOM: 1 * 50 µG
Supplier: US Biological


Description: 1,3-Dimethyl-1H-pyrazole-5-thiocarboxamide 97%
Catalog Number: APOSOR9683-5G
UOM: 1 * 5 g
Supplier: Apollo Scientific


Description: AzoDye-3 Carboxylic Acid is an excellent building block for labeling amino-containing molecules.
Catalog Number: AATB2470
UOM: 1 * 25 mg
Supplier: AAT BIOQUEST

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