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POR anticorps (C-Term) (DyLight 488)

Cet anticorps anti-POR est un anticorps Lapin Polyclonal détectant POR dans FACS. Adapté pour Humain.
N° du produit ABIN7354705

Aperçu rapide pour POR anticorps (C-Term) (DyLight 488) (ABIN7354705)

Antigène

Voir toutes POR Anticorps
POR (P450 (Cytochrome) Oxidoreductase (POR))

Reactivité

  • 46
  • 24
  • 20
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 41
  • 9
  • 2
  • 1
Lapin

Clonalité

  • 37
  • 16
Polyclonal

Conjugué

  • 35
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp POR est conjugé à/à la DyLight 488

Application

  • 36
  • 23
  • 10
  • 9
  • 7
  • 7
  • 7
  • 7
  • 2
  • 1
  • 1
  • 1
Flow Cytometry (FACS)
  • Épitope

    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    AA 633-668, C-Term

    Fonction

    Anti-Human POR DyLight® 488 conjugated Antibody

    Séquence

    RNMARDVQNT FYDIVAELGA MEHAQAVDYI KKLMTK

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

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

    Immunogène

    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.

    Isotype

    IgG
  • Indications d'application

    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.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Reconstitution

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

    Concentration

    Lot specific

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

    POR (P450 (Cytochrome) Oxidoreductase (POR))

    Autre désignation

    POR

    Sujet

    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.

    Poids moléculaire

    39 kDa

    ID gène

    5447

    UniProt

    P16435

    Pathways

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