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Image non disponible-APOSPC450573-1G

Hexakis(HFPO hexamer alkoxy)phosphazene

Numéro de catalogue: (APOSPC450573-1G)
Fournisseur: Apollo Scientific
Description: Hexakis(HFPO hexamer alkoxy)phosphazene
UOM: 1 * 1 g
Image non disponible-APOSPC3336-5G

Perfluoro-2,5,8,11,14-pentamethyl-3,6,9,12,15-pentaoxaoctadecanoic acid, methyl ester 97%

Fournisseur: Apollo Scientific
Description: Perfluoro-2,5,8,11,14-pentamethyl-3,6,9,12,15-pentaoxaoctadecanoic acid, methyl ester 97%

Image non disponible-BOSSBS-15444R-A647

Anti-MYH Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

Numéro de catalogue: (BOSSBS-15444R-A647)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-A750

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

Numéro de catalogue: (BOSSBS-15444R-A750)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-A350

Anti-MYH Rabbit Polyclonal Antibody (ALEXA FLUOR® 350)

Numéro de catalogue: (BOSSBS-15444R-A350)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-CY5

Anti-MYH Rabbit Polyclonal Antibody (Cy5)

Numéro de catalogue: (BOSSBS-15444R-CY5)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R

Anti-MYH Rabbit Polyclonal Antibody

Numéro de catalogue: (BOSSBS-15444R)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-CY7

Anti-MYH Rabbit Polyclonal Antibody (Cy7)

Numéro de catalogue: (BOSSBS-15444R-CY7)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-HRP

Anti-MYH Rabbit Polyclonal Antibody (HRP)

Numéro de catalogue: (BOSSBS-15444R-HRP)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-CY3

Anti-MYH Rabbit Polyclonal Antibody (Cy3)

Numéro de catalogue: (BOSSBS-15444R-CY3)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-FITC

Anti-MYH Rabbit Polyclonal Antibody (FITC)

Numéro de catalogue: (BOSSBS-15444R-FITC)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-A488

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

Numéro de catalogue: (BOSSBS-15444R-A488)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-A555

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

Numéro de catalogue: (BOSSBS-15444R-A555)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-15444R-A680

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

Numéro de catalogue: (BOSSBS-15444R-A680)
Fournisseur: Bioss
Description: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.
UOM: 1 * 100 µl
Image du produit-SO142

Random hexamer primer

Numéro de catalogue: (SO142)
Fournisseur: Thermo Fisher Scientific
Description: Random hexamer primer is a mixture of single-stranded random hexanucleotides with 5'- and 3'-hydroxyl ends. The primer is supplied as a ready to use, 20X concentrated aqueous solution. Random hexamer primer has been functionally tested in first strand cDNA synthesis.
UOM: 1 * 1 KIT

Certificats


Image non disponible-BOSSBS-9433R-CY5.5

Anti-FIGNL1 Rabbit Polyclonal Antibody (Cy5.5®)

Numéro de catalogue: (BOSSBS-9433R-CY5.5)
Fournisseur: Bioss
Description: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
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Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l'call est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
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