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Descripción: Ácido (±)-4-bromomandelico ≥98.0% (by GC, titration analysis)
Numero del catalogo: TCIAB0609-5G
UOM: 1 * 5 g
Proveedor: TCI


Descripción: tert-Butyl 2-bromoisobutyrate 97%
Numero del catalogo: L08216.09
UOM: 1 * 10 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Descripción: 6-Bromohexanoato de etilo ≥97%
Numero del catalogo: A18398.30
UOM: 1 * 250 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Descripción: Sodium bromodifluoroacetate ≥98.0% (by HPLC, titration analysis)
Numero del catalogo: TCIAS0908-5G
UOM: 1 * 5 g
Proveedor: TCI


Descripción: 6-Bromohexanoato de etilo 98%
Numero del catalogo: ACRO305920250
UOM: 1 * 25 g
Proveedor: Thermo Fisher Scientific

FDS


Descripción: X-GlcA is a substrate for b-Glucuronidase (GUS) encoded by the gusA gene. The substrate is used as a qualitative marker of specific GUS expression.
Numero del catalogo: APOSBIMB1021-1G
UOM: 1 * 1 g
Proveedor: Apollo Scientific


Descripción: Naphthol AS-BI-β-D-Glucuronide ≥98.0% (by HPLC, total nitrogen) for biochemical research
Numero del catalogo: TCIAN0882-25MG
UOM: 1 * 25 mg
Proveedor: TCI


Descripción: 3-(Methoxydimethylsilyl)propyl acrylate ≥95.0% (por GC) estabilizado
Numero del catalogo: TCIAM2525-5G
UOM: 1 * 5 g
Proveedor: TCI


Descripción: N,N-Bis(4-bromophenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline ≥98.0% (by HPLC, titration analysis)
Numero del catalogo: TCIAB4660-200MG
UOM: 1 * 200 mg
Proveedor: TCI


Descripción: A cell-permeable cGMP analog which is more resistant to phosphodiesterases than cGMP and which preferentially activates cGMP-dependent protein kinase. It inhibits thrombin stimulated arachidonic acid release in human platelets.
Numero del catalogo: ENZOBMLCN2050010
UOM: 1 * 10 mg
Proveedor: ENZO LIFE SCIENCES


Descripción: Members of the WD repeat protein family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis and gene regulation. BRWD3 (bromodomain and WD repeat-containing protein 3) is a 1,802 amino acid protein expressed in fetal liver and most adult tissues. Existing as five alternatively spliced isoforms, BRWD3 contains two bromo domains, nine WD repeats and is thought to play a role in transcription by modifying chromatin. Mutations in the gene encoding BRWD3 are the cause of mental retardation X-linked type 93 (MRX93), which is also known as mental retardation X-linked with macrocephaly (XLMR). MRX93 is characterized by mild intellectual disability, macrocephaly, a prominent forehead and large cupped ears.
Numero del catalogo: BOSSBS-11811R-FITC
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Members of the WD repeat protein family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis and gene regulation. BRWD3 (bromodomain and WD repeat-containing protein 3) is a 1802 amino acid protein expressed in fetal liver and most adult tissues. Existing as five alternatively spliced isoforms, BRWD3 contains two bromo domains, nine WD repeats and is thought to play a role in transcription by modifying chromatin. Mutations in the gene encoding BRWD3 are the cause of mental retardation X-linked type 93 (MRX93), which is also known as mental retardation X-linked with macrocephaly (XLMR). MRX93 is characterised by mild intellectual disability, macrocephaly, a prominent forehead and large cupped ears.
Numero del catalogo: BOSSBS-11811R-A750
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Members of the WD repeat protein family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis and gene regulation. BRWD3 (bromodomain and WD repeat-containing protein 3) is a 1,802 amino acid protein expressed in fetal liver and most adult tissues. Existing as five alternatively spliced isoforms, BRWD3 contains two bromo domains, nine WD repeats and is thought to play a role in transcription by modifying chromatin. Mutations in the gene encoding BRWD3 are the cause of mental retardation X-linked type 93 (MRX93), which is also known as mental retardation X-linked with macrocephaly (XLMR). MRX93 is characterized by mild intellectual disability, macrocephaly, a prominent forehead and large cupped ears.
Numero del catalogo: BOSSBS-11811R-A555
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Members of the WD repeat protein family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis and gene regulation. BRWD3 (bromodomain and WD repeat-containing protein 3) is a 1,802 amino acid protein expressed in fetal liver and most adult tissues. Existing as five alternatively spliced isoforms, BRWD3 contains two bromo domains, nine WD repeats and is thought to play a role in transcription by modifying chromatin. Mutations in the gene encoding BRWD3 are the cause of mental retardation X-linked type 93 (MRX93), which is also known as mental retardation X-linked with macrocephaly (XLMR). MRX93 is characterized by mild intellectual disability, macrocephaly, a prominent forehead and large cupped ears.
Numero del catalogo: BOSSBS-11811R-A350
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Members of the WD repeat protein family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis and gene regulation. BRWD3 (bromodomain and WD repeat-containing protein 3) is a 1,802 amino acid protein expressed in fetal liver and most adult tissues. Existing as five alternatively spliced isoforms, BRWD3 contains two bromo domains, nine WD repeats and is thought to play a role in transcription by modifying chromatin. Mutations in the gene encoding BRWD3 are the cause of mental retardation X-linked type 93 (MRX93), which is also known as mental retardation X-linked with macrocephaly (XLMR). MRX93 is characterized by mild intellectual disability, macrocephaly, a prominent forehead and large cupped ears.
Numero del catalogo: BOSSBS-11811R-A647
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Members of the WD repeat protein family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis and gene regulation. BRWD3 (bromodomain and WD repeat-containing protein 3) is a 1,802 amino acid protein expressed in fetal liver and most adult tissues. Existing as five alternatively spliced isoforms, BRWD3 contains two bromo domains, nine WD repeats and is thought to play a role in transcription by modifying chromatin. Mutations in the gene encoding BRWD3 are the cause of mental retardation X-linked type 93 (MRX93), which is also known as mental retardation X-linked with macrocephaly (XLMR). MRX93 is characterized by mild intellectual disability, macrocephaly, a prominent forehead and large cupped ears.
Numero del catalogo: BOSSBS-11811R-HRP
UOM: 1 * 100 µl
Proveedor: Bioss


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