d glc 13c6 Search Results


d glc 13c6  (MedChemExpress)
93
MedChemExpress d glc 13c6
D Glc 13c6, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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uniformly labelled d-glc-13c6  (Millipore)
90
Millipore uniformly labelled d-glc-13c6
Uniformly Labelled D Glc 13c6, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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u- 13 c 6 ]-glucose clm-1396 d-glc-u- 13 c 6  (Cambridge Isotope Laboratories)
90
Cambridge Isotope Laboratories u- 13 c 6 ]-glucose clm-1396 d-glc-u- 13 c 6
U 13 C 6 ] Glucose Clm 1396 D Glc U 13 C 6, supplied by Cambridge Isotope Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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d -[1,2- 13 c 2 ]glc  (Isotec Inc)
90
Isotec Inc d -[1,2- 13 c 2 ]glc
Predicted and measured relative abundance of mass isotopomers of C18:1 methyl ester, after growth on <t>[U-13C6]Glc</t> and <t>unlabeled</t> <t>Suc.</t> From the fragment C18:1(1-2), representing the terminal biosynthetic acetate unit, the distribution of mass isotopomers was predicted. The polymerization of nine acetate units to a C18 fatty acid molecule can be described by a binominal distribution (compare with Lee et al., 1992): (p + (q1 + q2))9. q1, Fraction of (13C1) acetate; q2, fraction of (13C2)-acetate; and p = 1 − q1 − q2, the fraction of (12C2) acetate. The expansion of this binominal distribution leads to the relative abundance of mass isotopomers (m0, m1, m2… m2n) of the fatty acid (Lee et al., 1992). After labeling with [U-13C6]Glc (diluted 20:80 with Suc, as related to hexose units), the fractional labeling in C18:1(1-2) was determined to q1 = 0.084, q2 = 0.267, and p = 0.649. This equals an average 13C content of 31%. The predicted distribution (white bars) and the measured molecular ion of C18:1 (black bars) are similar, indicating that the majority of fatty acid molecules was formed from acetate units labeled as measured in the fragment C18:1(1-2). However, a 4% fraction of fatty acid molecules was much higher labeled. Thus, during fatty acid biosynthesis, a small part of fatty acid molecules has been made mainly from labeled Glc, whereas the bulk of fatty acids was made by a homogeneous mixture of about 30% labeled and 60% unlabeled hexose units.
D [1,2 13 C 2 ]Glc, supplied by Isotec Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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u-[ 13 c 6 ]glucopyranoside  (Omicron Biochemicals Inc)
90
Omicron Biochemicals Inc u-[ 13 c 6 ]glucopyranoside
Predicted and measured relative abundance of mass isotopomers of C18:1 methyl ester, after growth on <t>[U-13C6]Glc</t> and <t>unlabeled</t> <t>Suc.</t> From the fragment C18:1(1-2), representing the terminal biosynthetic acetate unit, the distribution of mass isotopomers was predicted. The polymerization of nine acetate units to a C18 fatty acid molecule can be described by a binominal distribution (compare with Lee et al., 1992): (p + (q1 + q2))9. q1, Fraction of (13C1) acetate; q2, fraction of (13C2)-acetate; and p = 1 − q1 − q2, the fraction of (12C2) acetate. The expansion of this binominal distribution leads to the relative abundance of mass isotopomers (m0, m1, m2… m2n) of the fatty acid (Lee et al., 1992). After labeling with [U-13C6]Glc (diluted 20:80 with Suc, as related to hexose units), the fractional labeling in C18:1(1-2) was determined to q1 = 0.084, q2 = 0.267, and p = 0.649. This equals an average 13C content of 31%. The predicted distribution (white bars) and the measured molecular ion of C18:1 (black bars) are similar, indicating that the majority of fatty acid molecules was formed from acetate units labeled as measured in the fragment C18:1(1-2). However, a 4% fraction of fatty acid molecules was much higher labeled. Thus, during fatty acid biosynthesis, a small part of fatty acid molecules has been made mainly from labeled Glc, whereas the bulk of fatty acids was made by a homogeneous mixture of about 30% labeled and 60% unlabeled hexose units.
U [ 13 C 6 ]Glucopyranoside, supplied by Omicron Biochemicals Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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5.5 mm uniformly labeled 13 c-d-glucose ( 13 c 6 -glc)  (Millipore)
90
Millipore 5.5 mm uniformly labeled 13 c-d-glucose ( 13 c 6 -glc)
KEY RESOURCES TABLE
5.5 Mm Uniformly Labeled 13 C D Glucose ( 13 C 6 Glc), supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Predicted and measured relative abundance of mass isotopomers of C18:1 methyl ester, after growth on [U-13C6]Glc and unlabeled Suc. From the fragment C18:1(1-2), representing the terminal biosynthetic acetate unit, the distribution of mass isotopomers was predicted. The polymerization of nine acetate units to a C18 fatty acid molecule can be described by a binominal distribution (compare with Lee et al., 1992): (p + (q1 + q2))9. q1, Fraction of (13C1) acetate; q2, fraction of (13C2)-acetate; and p = 1 − q1 − q2, the fraction of (12C2) acetate. The expansion of this binominal distribution leads to the relative abundance of mass isotopomers (m0, m1, m2… m2n) of the fatty acid (Lee et al., 1992). After labeling with [U-13C6]Glc (diluted 20:80 with Suc, as related to hexose units), the fractional labeling in C18:1(1-2) was determined to q1 = 0.084, q2 = 0.267, and p = 0.649. This equals an average 13C content of 31%. The predicted distribution (white bars) and the measured molecular ion of C18:1 (black bars) are similar, indicating that the majority of fatty acid molecules was formed from acetate units labeled as measured in the fragment C18:1(1-2). However, a 4% fraction of fatty acid molecules was much higher labeled. Thus, during fatty acid biosynthesis, a small part of fatty acid molecules has been made mainly from labeled Glc, whereas the bulk of fatty acids was made by a homogeneous mixture of about 30% labeled and 60% unlabeled hexose units.

Journal:

Article Title: Probing in Vivo Metabolism by Stable Isotope Labeling of Storage Lipids and Proteins in Developing Brassica napus Embryos 1

doi: 10.1104/pp.004275

Figure Lengend Snippet: Predicted and measured relative abundance of mass isotopomers of C18:1 methyl ester, after growth on [U-13C6]Glc and unlabeled Suc. From the fragment C18:1(1-2), representing the terminal biosynthetic acetate unit, the distribution of mass isotopomers was predicted. The polymerization of nine acetate units to a C18 fatty acid molecule can be described by a binominal distribution (compare with Lee et al., 1992): (p + (q1 + q2))9. q1, Fraction of (13C1) acetate; q2, fraction of (13C2)-acetate; and p = 1 − q1 − q2, the fraction of (12C2) acetate. The expansion of this binominal distribution leads to the relative abundance of mass isotopomers (m0, m1, m2… m2n) of the fatty acid (Lee et al., 1992). After labeling with [U-13C6]Glc (diluted 20:80 with Suc, as related to hexose units), the fractional labeling in C18:1(1-2) was determined to q1 = 0.084, q2 = 0.267, and p = 0.649. This equals an average 13C content of 31%. The predicted distribution (white bars) and the measured molecular ion of C18:1 (black bars) are similar, indicating that the majority of fatty acid molecules was formed from acetate units labeled as measured in the fragment C18:1(1-2). However, a 4% fraction of fatty acid molecules was much higher labeled. Thus, during fatty acid biosynthesis, a small part of fatty acid molecules has been made mainly from labeled Glc, whereas the bulk of fatty acids was made by a homogeneous mixture of about 30% labeled and 60% unlabeled hexose units.

Article Snippet: d -[U- 13 C 6 ]Glc, d -[1,2- 13 C 2 ]Glc, and [U- 13 C 12 ]Suc (99% 13 C-enrichment) were purchased from Isotec (Miamisburg, OH).

Techniques: Labeling

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: Malic Enzyme Couples Mitochondria with Aerobic Glycolysis in Osteoblasts

doi: 10.1016/j.celrep.2020.108108

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: The cells were then incubated for 30 mins with cMEMα containing 5.5 mM uniformly labeled 13 C-D-glucose ( 13 C 6 -Glc) (Sigma, 389374) in lieu of regular glucose.

Techniques: Recombinant, Labeling, Cell Viability Assay, Colorimetric Assay, SYBR Green Assay