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Adenylosuccinate Lyase Antikörper (AA 1-484)

Name: Adenylosuccinate Lyase Antikörper (AA 1-484)
SKU: ABIN5776044
Price: 642.31 EUR
Availability: InStock

ADSL Reaktivität: Human WB, ELISA, IF, FACS, ICC Wirt: Maus Monoclonal AT16C10 unconjugated

The Recombinant Human ADSL (20ng) and Cell lysates (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human ADSL antibody (1:1000). (Adenylosuccinate Lyase Antikörper (AA 1-484))

ICC/IF analysis of ADSL in Hep3B cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human ADSL antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green). (Adenylosuccinate Lyase Antikörper (AA 1-484))

2 Abbildungen

Produktnummer ABIN5776044

Datenblatt (PDF)

Target Alle Adenylosuccinate Lyase (ADSL) Antikörper anzeigen

Adenylosuccinate Lyase (ADSL)
Bindungsspezifität
15

10

3

1

1

1

1

1
AA 1-484
Reaktivität
45

21

6

3

2

2

2

1

1

1

1
Human
Wirt
42

3
Maus
Passende Sekundärantikörper
Klonalität
43

1
Monoklonal
Konjugat
20

2

2

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1

1
Dieser Adenylosuccinate Lyase Antikörper ist unkonjugiert
Applikation
18

13

13

11

9

7

6

4

3

3

2

2

2

1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS), Immunocytochemistry (ICC)

Immunogen

Recombinant human ADSL(1-484aa) purified from E. coli

Klon

AT16C10

Isotyp

IgG1 kappa

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Beschränkungen

Nur für Forschungszwecke einsetzbar
Format

Liquid

Konzentration

1 mg/mL

Lagerung

4 °C,-20 °C,-80 °C

Informationen zur Lagerung

Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
Target

Adenylosuccinate Lyase (ADSL)

Andere Bezeichnung

Adenylosuccinate Lyase/ADSL (ADSL Produkte)

Hintergrund

Adenylosuccinate lyase, also known as ADSL, is an enzyme that converts adenylosuccinate to AMP and fumarate as part of the purine nucleotide cycle. Defects in ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency). ADSL deficiency is an autosomal recessive disorder characterized by the accumulation in the body fluids of succinylaminoimidazole-carboxamide riboside (SAICA-riboside) and succinyladenosine (S-Ado).

NCBI Accession

NP_000017

Pathways

Ribonucleoside Biosynthetic Process