Drucken

Sie suchten nach: ATTO+514+acid


121 648  Ergebnisse wurden gefunden

Suchergebnis einschränken: Sortieren nach
SearchResultCount:"121648"

Sort Results

Listenansicht Hybridansicht

Bewerten Sie das Suchergebnis

Image Unavailable-AATB2862

ATTO 514 acid

Artikel-Nr: (AATB2862)
Lieferant: AAT BIOQUEST INC
Beschreibung: ATTO 514 is a rhodamine-based fluorophore characterized by exceptional water solubility, strong absorption, high fluorescence quantum yield, and outstanding thermal and photo-stability.
VE: 1 * 10 mg

Neuer Artikel bei VWR!


Image Unavailable-AATB2864

ATTO 514 maleimide

Artikel-Nr: (AATB2864)
Lieferant: AAT BIOQUEST INC
Beschreibung: ATTO 514 is a rhodamine-based fluorescent labeling dye known for its favorable spectral qualities.
VE: 1 * 1 mg

Neuer Artikel bei VWR!


Image Unavailable-AATB2863

ATTO 514 NHS ester

Artikel-Nr: (AATB2863)
Lieferant: AAT BIOQUEST INC
Beschreibung: ATTO 514, a hydrophilic rhodamine-based fluorophore, is known for its excellent water solubility, strong absorption, high fluorescence quantum yield, and thermal and photo-stability.
VE: 1 * 1 mg

Neuer Artikel bei VWR!


Image Unavailable-42582.MD

Abietinsäure ≥90%

Lieferant: Thermo Scientific
Beschreibung: Abietinsäure ≥90%

Sicherheitsdatenblätter Zertifikate

Image Unavailable-L13770.14

Abietinsäure ≥75%, tech.

Lieferant: Thermo Scientific
Beschreibung: Abietinsäure ≥75%, tech.

Sicherheitsdatenblätter Zertifikate

Image Unavailable-BOSSBS-7707R-A680

Anti-ZBTB2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Artikel-Nr: (BOSSBS-7707R-A680)
Lieferant: Bioss
Beschreibung: The BTB (Broad-Complex, Tramtrack and Bric a brac) domain, also known as the POZ (Poxvirus and Zinc finger) domain, is an N-terminal homodimerisation domain that contains multiple copies of kelch repeats and/or C2H2-type zinc fingers. Proteins that contain BTB domains are thought to be involved in transcriptional regulation via control of chromatin structure and function. ZBTB1 (zinc finger and BTB domain containing 1), also known as KIAA0997, is a 713 amino acid nuclear protein that contains one BTB (POZ) domain and 8 C2H2-type zinc fingers. ZBTB2 is a 514 amino acid nuclear protein that contains one BTB (POZ) domain and 4 C2H2-type zinc fingers. ZBTB25, also known as ZNF46 or KUP, is a 435 amino acid nuclear protein that is expressed mainly in hematopoietic cells and testis and contains one BTB (POZ) domain and 2 C2H2-type zinc fingers.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-7740R-CY5.5

Anti-CFAP53 Rabbit Polyclonal Antibody (Cy5.5®)

Artikel-Nr: (BOSSBS-7740R-CY5.5)
Lieferant: Bioss
Beschreibung: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-7707R-A488

Anti-ZBTB2 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Artikel-Nr: (BOSSBS-7707R-A488)
Lieferant: Bioss
Beschreibung: The BTB (Broad-Complex, Tramtrack and Bric a brac) domain, also known as the POZ (Poxvirus and Zinc finger) domain, is an N-terminal homodimerization domain that contains multiple copies of kelch repeats and/or C2H2-type zinc fingers. Proteins that contain BTB domains are thought to be involved in transcriptional regulation via control of chromatin structure and function. ZBTB1 (zinc finger and BTB domain containing 1), also known as KIAA0997, is a 713 amino acid nuclear protein that contains one BTB (POZ) domain and 8 C2H2-type zinc fingers. ZBTB2 is a 514 amino acid nuclear protein that contains one BTB (POZ) domain and 4 C2H2-type zinc fingers. ZBTB25, also known as ZNF46 or KUP, is a 435 amino acid nuclear protein that is expressed mainly in hematopoietic cells and testis and contains one BTB (POZ) domain and 2 C2H2-type zinc fingers.
VE: 1 * 100 µl
Product Image-ACRO173130250

Abietinsäure 85%

Lieferant: Thermo Scientific
Beschreibung: Abietinsäure 85%

Sicherheitsdatenblätter

Image Unavailable-BOSSBS-7707R-A750

Anti-ZBTB2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Artikel-Nr: (BOSSBS-7707R-A750)
Lieferant: Bioss
Beschreibung: The BTB (Broad-Complex, Tramtrack and Bric a brac) domain, also known as the POZ (Poxvirus and Zinc finger) domain, is an N-terminal homodimerisation domain that contains multiple copies of kelch repeats and/or C2H2-type zinc fingers. Proteins that contain BTB domains are thought to be involved in transcriptional regulation via control of chromatin structure and function. ZBTB1 (zinc finger and BTB domain containing 1), also known as KIAA0997, is a 713 amino acid nuclear protein that contains one BTB (POZ) domain and 8 C2H2-type zinc fingers. ZBTB2 is a 514 amino acid nuclear protein that contains one BTB (POZ) domain and 4 C2H2-type zinc fingers. ZBTB25, also known as ZNF46 or KUP, is a 435 amino acid nuclear protein that is expressed mainly in hematopoietic cells and testis and contains one BTB (POZ) domain and 2 C2H2-type zinc fingers.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-7740R-A750

Anti-CCDC11 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Artikel-Nr: (BOSSBS-7740R-A750)
Lieferant: Bioss
Beschreibung: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-7740R-A555

Anti-CFAP53 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Artikel-Nr: (BOSSBS-7740R-A555)
Lieferant: Bioss
Beschreibung: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-7740R-A350

Anti-CFAP53 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Artikel-Nr: (BOSSBS-7740R-A350)
Lieferant: Bioss
Beschreibung: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-7740R-A647

Anti-CFAP53 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Artikel-Nr: (BOSSBS-7740R-A647)
Lieferant: Bioss
Beschreibung: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE: 1 * 100 µl
Image Unavailable-BWRLBS1135

Anti-GAD-67 Rabbit Polyclonal Antibody [clone: A492]

Artikel-Nr: (BWRLBS1135)
Lieferant: Bioworld Technology
Beschreibung: Synthetic peptide, corresponding to amino acids 460-514 of Human GAD-67.
VE: 1 * 100 µG
Image Unavailable-BOSSBS-7740R-HRP

Anti-CFAP53 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Artikel-Nr: (BOSSBS-7740R-HRP)
Lieferant: Bioss
Beschreibung: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE: 1 * 100 µl
Preis auf Anfrage
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 1-800-932 - 5000.
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 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt, lassen Sie sich gegebenenfalls ein Angebot zum Artikel erstellen.
Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Der mit diesem Symbol gekennzeichnete Artikel wird aus dem Programm genommen. Er ist nur noch bis zum Ende des Lagerbestands verfügbar. Sicher haben wir aber eine Alternative im Sortiment. Bei der Suche unterstützen wir Sie gerne! Wenden Sie sich dafür einfach an Ihre Ansprechpartner im Customer Service, Ihren Account Manager, Ihren Produktspezialisten oder unter 06151/39720 an unsere Zentrale in Darmstadt.
1 - 16 of 121 648
no targeter for Bottom