Print…

U heeft gezocht op: 3,4-Dichloroisothiazole-5-carboxylic+acid


147 162  results were found

Verfijn resultaten Sorteren bij
SearchResultCount:"147162"

Sort Results

List view Easy View (new)

Rate These Search Results

Image Unavailable-TCIAB5831-200MG

Benzyl 7-Oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate ≥97.0% (by GC)

Leverancier: TCI
Omschrijving: Benzyl 7-Oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate ≥97.0% (by GC)

Image Unavailable-TCIAM2479-100MG

Moxifloxacin hydrochloride monohydrate ≥98.0% (by HPLC, titration analysis)

Leverancier: TCI
Omschrijving: Moxifloxacin hydrochloride monohydrate ≥98.0% (by HPLC, titration analysis)

Image Unavailable-TCIAF1183-250MG

(Fmoc-amino)-PEG6-carboxylic acid ≥98.0% (by HPLC, titration analysis)

Catalogus nummer: (TCIAF1183-250MG)
Leverancier: TCI
Omschrijving: (Fmoc-amino)-PEG6-carboxylic acid ≥98.0% (by HPLC, titration analysis)
UOM: 1 * 250 mg
Image Unavailable-TCIAB5352-1G

Methyl (R)-(+)-3-boc-2,2-dimethyl-4-oxazolidinecarboxylate ≥96.0% (by GC)

Leverancier: TCI
Omschrijving: Methyl (R)-(+)-3-boc-2,2-dimethyl-4-oxazolidinecarboxylate ≥96.0% (by GC)

Image Unavailable-ENZOALX350101M100

Catharanthine tartrate (from Catharanthus roseus) ≥90% (dry basis)

Catalogus nummer: (ENZOALX350101M100)
Leverancier: ENZO LIFE SCIENCES
Omschrijving: Starting material for the synthesis of the antitumor drugs vinblastine and vincristine. It is less active as an inhibitor of tubulin self-assembly into microtubules than the latter two compounds.
UOM: 1 * 100 mg
Image Unavailable-TCIAE1131-1G

Ethyl-6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate ≥98.0% (by HPLC, total nitrogen)

Leverancier: TCI
Omschrijving: Ethyl-6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate ≥98.0% (by HPLC, total nitrogen)

Image Unavailable-ENZOALX270503MC05

trans-Ned-19

Leverancier: ENZO LIFE SCIENCES
Omschrijving: trans-Ned-19

Image Unavailable-APOSOR1755-25G

tert-Butyl-4-(2-aminoethyl)piperazine-1-carboxylate

Catalogus nummer: (APOSOR1755-25G)
Leverancier: Apollo Scientific
Omschrijving: tert-Butyl-4-(2-aminoethyl)piperazine-1-carboxylate
UOM: 1 * 25 g
Image Unavailable-APOSOR321497-250MG

(1S,3R)-3-(tert-Butoxycarbonylamino)cyclohexanecarboxylic acid

Catalogus nummer: (APOSOR321497-250MG)
Leverancier: Apollo Scientific
Omschrijving: (1S,3R)-3-(tert-Butoxycarbonylamino)cyclohexanecarboxylic acid
UOM: 1 * 250 mg
Image Unavailable-TCIAB3539-1G

(1S,3R)-3-(tert-Butoxycarbonylamino)cyclohexanecarboxylic acid ≥97.0% (by GC, titration analysis)

Catalogus nummer: (TCIAB3539-1G)
Leverancier: TCI
Omschrijving: (1S,3R)-3-(tert-Butoxycarbonylamino)cyclohexanecarboxylic acid ≥97.0% (by GC, titration analysis)
UOM: 1 * 1 g
Image Unavailable-BOSSBS-13126R-A488

Anti-EYA4 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalogus nummer: (BOSSBS-13126R-A488)
Leverancier: Bioss
Omschrijving: 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).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13126R-A555

Anti-EYA4 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalogus nummer: (BOSSBS-13126R-A555)
Leverancier: Bioss
Omschrijving: 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).
UOM: 1 * 100 µl
Image Unavailable-MAYBCC01601.250

Piperonylic acid

Catalogus nummer: (MAYBCC01601.250)
Leverancier: Thermo Scientific
Omschrijving: Piperonylic acid
UOM: 1 * 250 mg

Market Source Item This is a MarketSource item. Additional charges may apply

Image Unavailable-BOSSBS-13126R-A680

Anti-EYA4 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalogus nummer: (BOSSBS-13126R-A680)
Leverancier: Bioss
Omschrijving: 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).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13126R-A647

Anti-EYA4 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalogus nummer: (BOSSBS-13126R-A647)
Leverancier: Bioss
Omschrijving: 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).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13126R-A750

Anti-EYA4 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalogus nummer: (BOSSBS-13126R-A750)
Leverancier: Bioss
Omschrijving: 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).
UOM: 1 * 100 µl
Bel voor prijs
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dit artikel is geblokkeerd voor uw organisatie. Neem contact op met uw inkoopafdeling voor meer informatie
Het orginele artikel is niet langer beschikbaar. Het alternatief dat wordt getoond is beschikbaar
Product(en) gemarkeerd met dit symbool worden niet meer verkocht cq verkocht tot het einde van de voorraad. Alternatieven zijn mogelijk beschikbaar door te zoeken met het VWR-catalogusnummer dat hierboven wordt vermeld. Voor meer informatie kunt u contact opnemen met customer service: 020-4808410.
129 - 144 of 147 162
no targeter for Bottom