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Opis: Anti-Wolf-Hirschhorn Syndrome Candidate 2 Protein Chicken Polyclonal Antibody
Katalógové číslo: USBIW0485-01
Merná jednotka: 1 * 50 µG
Dodávateľ: UNITED BIOCHEMICALS


Opis: Anti-Wolf-Hirschhorn Syndrome Candidate 2 Protein Chicken Polyclonal Antibody
Katalógové číslo: USBIW0485-02
Merná jednotka: 1 * 50 µG
Dodávateľ: UNITED BIOCHEMICALS


Opis: Anti-Wolf-Hirschhorn Syndrome Candidate 1-like 1 Mouse Monoclonal Antibody [clone: 8G3]
Katalógové číslo: USBIW0484-100
Merná jednotka: 1 * 100 µl
Dodávateľ: UNITED BIOCHEMICALS


Opis: Anti-WHSC1L1 Mouse Polyclonal Antibody
Katalógové číslo: USBI135380
Merná jednotka: 1 * 50 µG
Dodávateľ: UNITED BIOCHEMICALS


Opis: CELLCYTE X™ offers the user the ability to image live cells in real-time from within the incubator. From all of these images, the user can fully understand and review cell kinetic trends at any point in time with user-friendly analysis software.
Katalógové číslo: 630-3521
Merná jednotka: 1 * 1 items
Dodávateľ: DISCOVER ECHO


Opis: The LETM1 is a factor of the mitochondrial K+ homeostasis with a potential role in the Wolf-Hirschhorn syndrome.
Katalógové číslo: PRSI30-247
Merná jednotka: 1 * 100 µG
Dodávateľ: PROSCI


Opis: This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. The function of the protein has not been determined. Two alternatively spliced variants have been described.
Katalógové číslo: PRSI56-628
Merná jednotka: 1 * 400 µl
Dodávateľ: PROSCI


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.
Katalógové číslo: BOSSBS-15591R-A647
Merná jednotka: 1 * 100 µl
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.
Katalógové číslo: BOSSBS-15591R-A750
Merná jednotka: 1 * 100 µl
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.
Katalógové číslo: BOSSBS-15591R-FITC
Merná jednotka: 1 * 100 µl
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.
Katalógové číslo: BOSSBS-15591R-CY7
Merná jednotka: 1 * 100 µl
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.
Katalógové číslo: BOSSBS-15591R-CY3
Merná jednotka: 1 * 100 µl
Dodávateľ: BIOSS INC


Opis: This gene encodes a protein that is localized 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. [provided by RefSeq, Oct 2009].
Katalógové číslo: BOSSBS-15591R
Merná jednotka: 1 * 100 µl
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.
Katalógové číslo: BOSSBS-15591R-HRP
Merná jednotka: 1 * 100 µl
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.
Katalógové číslo: BOSSBS-15591R-CY5
Merná jednotka: 1 * 100 µl
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.
Katalógové číslo: BOSSBS-15591R-A350
Merná jednotka: 1 * 100 µl
Dodávateľ: BIOSS INC