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Image Unavailable-BOSSBS-11769R-FITC

Anti-TIMM8A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-11769R-FITC)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11769R-A555

Anti-TIMM8A Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-11769R-A555)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11769R-CY7

Anti-TIMM8A Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-11769R-CY7)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11769R

Anti-TIMM8A Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-11769R)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
Image Unavailable-319333-2L

Potassium hydroxide 0.1 M (0.1 N) in methanol ≥99% volumetric solution, Fluka™

Catalog Number: (319333-2L)
Supplier: Honeywell Chemicals
Description: Potassium hydroxide 0.1 M (0.1 N) in methanol ≥99% volumetric solution, Fluka™
UOM: 1 * 2 L

SDS


Image Unavailable-MOLEM39889137

Perfluorooctane

Catalog Number: (MOLEM39889137)
Supplier: Molekula
Description: Perfluorooctane
UOM: 1 * 5 g

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

Image Unavailable-APOSOR451156-1G

1-(1,4-Dioxaspiro[4.5]dec-8-yl)-ethanone

Catalog Number: (APOSOR451156-1G)
Supplier: Apollo Scientific
Description: 1-(1,4-Dioxaspiro[4.5]dec-8-yl)-ethanone
UOM: 1 * 1 g
Image Unavailable-BOSSBS-11769R-A488

Anti-TIMM8A Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-11769R-A488)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
Image Unavailable-APOSOR471172-5G

7-Methyl-1,4-dioxaspiro[4.5]decan-8-one

Catalog Number: (APOSOR471172-5G)
Supplier: Apollo Scientific
Description: 7-Methyl-1,4-dioxaspiro[4.5]decan-8-one
UOM: 1 * 5 g
Image Unavailable-APOSOR451157-250MG

1,4-Dioxaspiro[4.5]decane-8,8-dimethanol

Supplier: Apollo Scientific
Description: 1,4-Dioxaspiro[4.5]decane-8,8-dimethanol

Image Unavailable-APOSPC402041-250MG

8-(Trifluoromethyl)-1,4-dioxaspiro[4.5]decan-8-ol

Catalog Number: (APOSPC402041-250MG)
Supplier: Apollo Scientific
Description: 8-(Trifluoromethyl)-1,4-dioxaspiro[4.5]decan-8-ol
UOM: 1 * 250 mg
Image Unavailable-EHERL11693000ME

Organic reference standard, Caffeine 10 µg/ml in methanol, Dr Ehrenstorfer

Catalog Number: (EHERL11693000ME)
Supplier: EHRENSTORFER
Description: Organic Standard, Caffeine 10 µg/ml in methanol, Pack type: Glass bottle
UOM: 1 * 10 mL
Image Unavailable-EHERL12241000ME

Organic reference standard, 2,4-Dibromophenol 10 µg/ml in methanol, Dr Ehrenstorfer

Catalog Number: (EHERL12241000ME)
Supplier: EHRENSTORFER
Description: Organic Standard, 2,4-Dibromophenol 10 µg/ml in methanol, Pack type: Glass bottle
UOM: 1 * 10 mL
Image Unavailable-BOSSBS-11769R-A647

Anti-TIMM8A Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-11769R-A647)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11769R-CY3

Anti-TIMM8A Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-11769R-CY3)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11769R-CY5

Anti-TIMM8A Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-11769R-CY5)
Supplier: Bioss
Description: The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
UOM: 1 * 100 µl
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