Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

PLOD1 Antikörper (AA 23-640)

Dieses Anti-PLOD1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von PLOD1 in WB und ELISA. Geeignet für Human.
Produktnummer ABIN7600763

Kurzübersicht für PLOD1 Antikörper (AA 23-640) (ABIN7600763)

Target

Alle PLOD1 Antikörper anzeigen
PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))

Reaktivität

  • 17
  • 1
Human

Wirt

  • 14
  • 4
Kaninchen

Klonalität

  • 15
  • 3
Polyklonal

Konjugat

  • 13
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser PLOD1 Antikörper ist unkonjugiert

Applikation

  • 18
  • 12
  • 10
  • 8
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Bindungsspezifität

    • 8
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 23-640

    Verwendungszweck

    Anti-PLOD1 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross reactivity with other proteins.

    Produktmerkmale

    Anti-PLOD1 Antibody Picoband® (ABIN7600763). Tested in ELISA, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human PLOD1 recombinant protein (Position: K23-A640).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Al-Gazali, L. I., Bakalinova, D., Varady, E., Scorer, J., Nork, M. Further delineation of Nevo syndrome. J. Med. Genet. 34: 366-370, 1997. 2. Brinckmann, J., Acil, Y., Feshchenko, S., Katzer, E., Brenner, R., Kulozik, A., Kugler, S. Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C). Arch. Derm. Res. 290: 181-186, 1998. 3. Dembure, P. P., Janko, A. R., Priest, J. H., Elsas, L. J. Ascorbate regulation of collagen biosynthesis in Ehlers-Danlos syndrome, type VI. Metabolism 36: 687-691, 1987.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Konzentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))

    Andere Bezeichnung

    PLOD1

    Hintergrund

    Synonyms: 70 kDa ribosomal protein S6 kinase 1 antibody, KS6B1_HUMAN antibody, p70 alpha antibody, P70 beta 1 antibody, p70 ribosomal S6 kinase alpha antibody, p70 ribosomal S6 kinase beta 1 antibody, p70 S6 kinase alpha antibody, P70 S6 Kinase antibody, p70 S6 kinase alpha 1 antibody, p70 S6 kinase alpha 2 antibody, p70 S6K antibody, p70 S6K-alpha antibody, p70 S6KA antibody, p70(S6K) alpha antibody, p70(S6K)-alpha antibody, p70-alpha antibody, p70-S6K 1 antibody, p70-S6K antibody, P70S6K antibody, P70S6K1 antibody, p70S6Kb antibody, PS6K antibody, Ribosomal protein S6 kinase 70 kDa polypeptide 1 antibody, Ribosomal protein S6 kinase beta 1 antibody, Ribosomal protein S6 kinase beta-1 antibody, Ribosomal protein S6 kinase I antibody, RPS6KB1 antibody, S6K antibody, S6K-beta-1 antibody, S6K1 antibody, Serine/threonine kinase 14 alpha antibody, Serine/threonine-protein kinase 14A antibody, STK14A antibody

    Tissue Specificity: Expressed in all tissues.

    Background: Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity. Two transcript variants encoding different isoforms have been found for this gene.

    Molekulargewicht

    84 kDa

    Gen-ID

    5351

    UniProt

    Q02809
Sie sind hier:
Chat with us!