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POR antibody (C-Term)

The Mouse Monoclonal anti-POR antibody is suitable to detect POR in samples from Human. It has been validated for WB, FACS and IHC (p).
Catalog No. ABIN7877442
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for POR antibody (C-Term) (ABIN7877442)

Target

See all POR Antibodies
POR (P450 (Cytochrome) Oxidoreductase (POR))

Reactivity

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  • 4
  • 4
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Human

Host

  • 54
  • 8
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Mouse

Clonality

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Monoclonal

Conjugate

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This POR antibody is un-conjugated

Application

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Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

7F5
  • Binding Specificity

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    C-Term

    Purpose

    Cytochrome P450 Reductase Antibody / POR / CYPOR

    Sequence

    RNMARDVQNT FYDIVAELGA MEHAQAVDYI KKLMTK

    Purification

    Antigen affinity purified

    Immunogen

    C-terminal region amino acids RNMARDVQNTFYDIVAELGAMEHAQAVDYIKKLMTK from the human protein were used as the immunogen for the Cytochrome P450 Reductase antibody.

    Isotype

    IgG2b
  • Application Notes

    Optimal dilution of the Cytochrome P450 Reductase antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Cytochrome P450 Reductase antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    POR (P450 (Cytochrome) Oxidoreductase (POR))

    Alternative Name

    Cytochrome P450 Reductase

    Background

    POR is a membrane-bound enzyme required for electron transfer from NADPH to cytochrome P450 in the endoplasmic reticulum of the eukaryotic 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 directly 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.

    UniProt

    P16435

    Pathways

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