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Image Unavailable-BOSSBS-9517R-CY5.5

Anti-AMPD3 Rabbit Polyclonal Antibody (Cy5.5®)

Artikel-Nr: (BOSSBS-9517R-CY5.5)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-CY5.5
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R-A647

Anti-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Artikel-Nr: (BOSSBS-9517R-A647)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-A647
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl

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Image Unavailable-BOSSBS-9517R-HRP

Anti-AMPD3 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Artikel-Nr: (BOSSBS-9517R-HRP)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-HRP
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R-A488

Anti-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Artikel-Nr: (BOSSBS-9517R-A488)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-A488
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-20136R-A750

Anti-BPNT1 Rabbit Polyclonal Antibody (ALEXA FLUOR® 750)

Artikel-Nr: (BOSSBS-20136R-A750)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-20136R-A750
Beschreibung: Converts adenosine 3'-phosphate 5'-phosphosulfate (PAPS) to adenosine 5'-phosphosulfate (APS) and 3'(2')-phosphoadenosine 5'- phosphate (PAP) to AMP. Has 1000-fold lower activity towards inositol 1,4-bisphosphate (Ins(1,4)P2) and inositol 1,3,4-trisphosphate (Ins(1,3,4)P3), but does not hydrolyse Ins(1)P, Ins(3,4)P2, Ins(1,3,4,5)P4 or InsP6.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R

Anti-AMPD3 Rabbit Polyclonal Antibody

Artikel-Nr: (BOSSBS-9517R)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R-CY7

Anti-AMPD3 Rabbit Polyclonal Antibody (Cy7®)

Artikel-Nr: (BOSSBS-9517R-CY7)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-CY7
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R-A350

Anti-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Artikel-Nr: (BOSSBS-9517R-A350)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-A350
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R-CY5

Anti-AMPD3 Rabbit Polyclonal Antibody (Cy5®)

Artikel-Nr: (BOSSBS-9517R-CY5)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-CY5
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R-CY3

Anti-AMPD3 Rabbit Polyclonal Antibody (Cy3®)

Artikel-Nr: (BOSSBS-9517R-CY3)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-CY3
Beschreibung: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6248R-A680

Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Artikel-Nr: (BOSSBS-6248R-A680)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-6248R-A680
Beschreibung: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localised to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6248R-CY3

Anti-IMPAD1 Rabbit Polyclonal Antibody (Cy3®)

Artikel-Nr: (BOSSBS-6248R-CY3)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-6248R-CY3
Beschreibung: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6248R

Anti-IMPAD1 Rabbit Polyclonal Antibody

Artikel-Nr: (BOSSBS-6248R)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-6248R
Beschreibung: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6248R-FITC

Anti-IMPAD1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Artikel-Nr: (BOSSBS-6248R-FITC)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-6248R-FITC
Beschreibung: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6248R-A555

Anti-IMPAD1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Artikel-Nr: (BOSSBS-6248R-A555)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-6248R-A555
Beschreibung: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9517R-A750

Anti-AMPD3 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Artikel-Nr: (BOSSBS-9517R-A750)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-9517R-A750
Beschreibung: AMP deaminase plays a critical role in energy metabolism. Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterised by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
UOM: 1 * 100 µl
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Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 044 745 13 13.
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