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Image Unavailable-BOSSBS-15484R-A750

Anti-HIBCH Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

Catalogus nummer: (BOSSBS-15484R-A750)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R-HRP

Anti-HIBCH Rabbit Polyclonal Antibody (HRP)

Catalogus nummer: (BOSSBS-15484R-HRP)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R-A555

Anti-HIBCH Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

Catalogus nummer: (BOSSBS-15484R-A555)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R-A680

Anti-HIBCH Rabbit Polyclonal Antibody (ALEXA FLUOR® 680)

Catalogus nummer: (BOSSBS-15484R-A680)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R-A488

Anti-HIBCH Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

Catalogus nummer: (BOSSBS-15484R-A488)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R

Anti-HIBCH Rabbit Polyclonal Antibody

Catalogus nummer: (BOSSBS-15484R)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localizing to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyzes HIBYL-CoA, a saline catabolite, and β-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of β-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterized by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R-CY7

Anti-HIBCH Rabbit Polyclonal Antibody (Cy7)

Catalogus nummer: (BOSSBS-15484R-CY7)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R-CY5

Anti-HIBCH Rabbit Polyclonal Antibody (Cy5)

Catalogus nummer: (BOSSBS-15484R-CY5)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15484R-FITC

Anti-HIBCH Rabbit Polyclonal Antibody (FITC)

Catalogus nummer: (BOSSBS-15484R-FITC)
Leverancier: Bioss
Omschrijving: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.
UOM: 1 * 100 µl
Image Unavailable-CAYM14805-500

2,2-Diphenyl-1-picrylhydrazyl (free radical) ≥95%, crystalline solid

Leverancier: Cayman Chemical
Omschrijving: DPPH, known formally as 2,2-diphenyl-1-picrylhydrazyl, is a cell-permeable, stable free radical that is commonly used to evaluate the ability of compounds to act as free radical scavengers or hydrogen donors and to measure the antioxidant activity of tissue extracts.

Product Image-663-0348

VWR® HCO 304, geleidbaarheidsmeter, handheld

Catalogus nummer: (663-0348)
Leverancier: VWR Collection
Omschrijving: Dit nauwkeurige apparaat, dat wordt gebruikt voor het meten van de geleidbaarheid tot 100 mS/cm, wordt geleverd met een duurzame grafietmeetcel met groot bereik voor universeel gebruik van DI-water tot zout water.
UOM: 1 * 1 ST
Product Image-663-8122

Geleidbaarheidsmeters, draagbaar, Cond 3110 / 3310

Leverancier: WTW
Omschrijving: Waterdichte handmeters ontworpen voor onbeperkt buitengebruik.

Image Unavailable-22.02.9.010.22

Saline solutions

Catalogus nummer: (22.02.9.010.22)
Leverancier: BALIS
Omschrijving: Cell culture buffer, Physiological saline solution, 9 ml, no standards
UOM: 1 * 100 ST

Certificaten


Image Unavailable-J60764.K2

TRIS-buffered saline (TBS, 10X) pH 7,4

Leverancier: Thermo Fisher Scientific
Omschrijving: Washing buffer, TRIS-buffered saline (TBS, 10X)

MSDS Certificaten

Image Unavailable-J60877.K2

TRIS-buffered saline (TBS, 20X) pH 7,4

Leverancier: Thermo Fisher Scientific
Omschrijving: Washing buffer, TRIS-buffered saline (TBS, 20X)

MSDS Certificaten

Image Unavailable-J62662.K7

TRIS-buffered saline (TBS, 10X) pH 7,6

Leverancier: Thermo Fisher Scientific
Omschrijving: Washing buffer, TRIS-buffered saline (TBS, 10X)

MSDS Certificaten

Bel voor prijs
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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.
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