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Katalógové číslo: (PRSI25-919)
Dodávateľ: PROSCI
Opis: SLC25A21 is a homolog of the S. cerevisiae ODC proteins, mitochondrial carriers that transport C5-C7 oxodicarboxylates across inner mitochondrial membranes. One of the species transported by ODC is 2-oxoadipate, a common intermediate in the catabolism of lysine, tryptophan, and hydroxylysine in mammals. Within mitochondria, 2-oxoadipate is converted into acetyl-CoA.SLC25A21 is a homolog of the S. cerevisiae ODC proteins, mitochondrial carriers that transport C5-C7 oxodicarboxylates across inner mitochondrial membranes. One of the species transported by ODC is 2-oxoadipate, a common intermediate in the catabolism of lysine, tryptophan, and hydroxylysine in mammals. Within mitochondria, 2-oxoadipate is converted into acetyl-CoA.
Merná jednotka: 1 * 50 µG


Katalógové číslo: (BOSSBS-15591R-FITC)
Dodávateľ: BIOSS INC
Opis: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-3221R-CY3)
Dodávateľ: BIOSS INC
Opis: HP1 gamma appears to be involved in transcriptional silencing in heterochromatin-like complexes. It recognizes and binds histone H3 tails methylated at 'Lys-9', leading to epigenetic repression. HP1 gamma may contribute to the association of the heterochromatin with the inner nuclear membrane through its interaction with lamin B receptor (LBR) and involved in the formation of functional kinetochore through interaction with MIS12 complex proteins.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-3221R-CY7)
Dodávateľ: BIOSS INC
Opis: HP1 gamma appears to be involved in transcriptional silencing in heterochromatin-like complexes. It recognizes and binds histone H3 tails methylated at 'Lys-9', leading to epigenetic repression. HP1 gamma may contribute to the association of the heterochromatin with the inner nuclear membrane through its interaction with lamin B receptor (LBR) and involved in the formation of functional kinetochore through interaction with MIS12 complex proteins.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-7998R-A680)
Dodávateľ: BIOSS INC
Opis: The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-6551R-A750)
Dodávateľ: BIOSS INC
Opis: NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-6551R-HRP)
Dodávateľ: BIOSS INC
Opis: NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-6551R-A488)
Dodávateľ: BIOSS INC
Opis: NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-3221R-FITC)
Dodávateľ: BIOSS INC
Opis: HP1 gamma appears to be involved in transcriptional silencing in heterochromatin-like complexes. It recognizes and binds histone H3 tails methylated at 'Lys-9', leading to epigenetic repression. HP1 gamma may contribute to the association of the heterochromatin with the inner nuclear membrane through its interaction with lamin B receptor (LBR) and involved in the formation of functional kinetochore through interaction with MIS12 complex proteins.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-7998R-FITC)
Dodávateľ: BIOSS INC
Opis: The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012].
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-3221R-CY5)
Dodávateľ: BIOSS INC
Opis: HP1 gamma appears to be involved in transcriptional silencing in heterochromatin-like complexes. It recognizes and binds histone H3 tails methylated at 'Lys-9', leading to epigenetic repression. HP1 gamma may contribute to the association of the heterochromatin with the inner nuclear membrane through its interaction with lamin B receptor (LBR) and involved in the formation of functional kinetochore through interaction with MIS12 complex proteins.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-3221R-A680)
Dodávateľ: BIOSS INC
Opis: HP1 gamma appears to be involved in transcriptional silencing in heterochromatin-like complexes. It Recognises and binds histone H3 tails methylated at 'Lys-9', leading to epigenetic repression. HP1 gamma may contribute to the association of the heterochromatin with the inner nuclear membrane through its interaction with lamin B receptor (LBR) and involved in the formation of functional kinetochore through interaction with MIS12 complex proteins.
Merná jednotka: 1 * 100 µl


Dodávateľ: Portwest
Opis: Ideal for cool outdoor conditions this jacket offers great function and style. The inner Sherpa pile lining traps warmth around the torso area, while lightly padded sleeves reduce bulk and allow great reach and movement.

Katalógové číslo: (BOSSBS-7998R-A647)
Dodávateľ: BIOSS INC
Opis: The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012].
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-7998R-A488)
Dodávateľ: BIOSS INC
Opis: The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012].
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-7998R-HRP)
Dodávateľ: BIOSS INC
Opis: The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012].
Merná jednotka: 1 * 100 µl


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