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POR Antikörper (C-Term) (DyLight 488)

Dieses Anti-POR-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von POR in FACS. Geeignet für Human.
Produktnummer ABIN7354705

Kurzübersicht für POR Antikörper (C-Term) (DyLight 488) (ABIN7354705)

Target

Alle POR Antikörper anzeigen
POR (P450 (Cytochrome) Oxidoreductase (POR))

Reaktivität

  • 52
  • 28
  • 23
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 47
  • 10
  • 2
  • 1
Kaninchen

Klonalität

  • 43
  • 17
Polyklonal

Konjugat

  • 42
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Dieser POR Antikörper ist konjugiert mit DyLight 488

Applikation

  • 43
  • 28
  • 14
  • 10
  • 9
  • 9
  • 9
  • 8
  • 2
  • 2
  • 1
  • 1
Flow Cytometry (FACS)
  • Bindungsspezifität

    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 633-668, C-Term

    Verwendungszweck

    Anti-Human POR DyLight® 488 conjugated Antibody

    Sequenz

    RNMARDVQNT FYDIVAELGA MEHAQAVDYI KKLMTK

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-Human POR DyLight® 488 conjugated Antibody -Dyl488. Tested in Flow Cytometry applications. This antibody reacts with Human.

    Immunogen

    A synthetic peptide corresponding to a sequence at the C-terminus of human POR , different from the related mouse and rat sequences by five amino acids.

    Isotyp

    IgG
  • Applikationshinweise

    Flow Cytometry (Fixed), 1-3 μg/1x106 cells1. Adachi, M., Asakura, Y., Matsuo, M., Yamamoto, T., Hanaki, K., Arlt, W. POR R457H is a global founder mutation causing Antley-Bixler syndrome with autosomal recessive trait. (Letter) Am. J. Med. Genet. 140A: 633-635, 2006. 2. Miller, W. L. Congenital adrenal hyperplasia. (Letter) New Eng. J. Med. 314: 1321-1322, 1986. 3. Shephard, E. A., Phillips, I. R., Santisteban, I., West, L. F., Palmer, C. N., Ashworth, A., Povey, S. Isolation of a human cytochrome P-450 reductase cDNA clone and localization of the corresponding gene to chromosome 7q11.2. Ann. Hum. Genet. 53: 291-301, 1989.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Rekonstitution

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

    Konzentration

    Lot specific

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
  • Target

    POR (P450 (Cytochrome) Oxidoreductase (POR))

    Andere Bezeichnung

    POR

    Hintergrund

    Synonyms: NADPH--cytochrome P450 reductase

    Tissue Specificity: Highly expressed in adult liver, lung and spleen than in corresponding fetal tissue. Also expressed in the lymph node, placenta, spinal cord and heart tissues. Expression is more elevated in peripheral blood leukocytes than in the bone marrow and in normal cells than malignant cells. Expressed at low levels in the early development of the hematopoietic system and in the promonocytic stage and at high levels in mature monocytes. Strongly expressed in acute inflammatory lesions caused by bacteria and fungi. Isoform 2 was detected in the lung, liver and mature monocytes.

    Background: POR is a membrane-boundenzyme required for electron transfer from NADPH to cytochrome P450 in the endoplasmic reticulum of theeukaryotic cell. The gene encodes an endoplasmic reticulum membrane oxidoreductase with an FAD-binding domain and a flavodoxin-like domain. The protein binds two cofactors, FAD and FMN, which allow it to donate electrons ly from NADPH to all microsomal P450 enzymes. Mutations in this gene have been associated with various diseases, including apparent combined P450C17 and P450C21 deficiency, amenorrhea and disordered steroidogenesis, congenital adrenal hyperplasia and Antley-Bixler syndrome.

    Molekulargewicht

    39 kDa

    Gen-ID

    5447

    UniProt

    P16435

    Pathways

    Regulation of Hormone Metabolic Process, Regulation of Hormone Biosynthetic Process, SARS-CoV-2 Protein Interaktom
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