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MED12 anticorps (AA 752-1974)

L’anticorps Lapin Polyclonal anti-MED12 a été validé pour ELISA et WB. Il convient pour détecter MED12 dans des échantillons de Humain.
N° du produit ABIN7602421

Aperçu rapide pour MED12 anticorps (AA 752-1974) (ABIN7602421)

Antigène

Voir toutes MED12 Anticorps
MED12 (Mediator Complex Subunit 12 (MED12))

Reactivité

  • 29
  • 23
  • 17
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 38
  • 1
  • 1
Lapin

Clonalité

  • 39
  • 1
Polyclonal

Conjugué

  • 16
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MED12 est non-conjugé

Application

  • 25
  • 14
  • 13
  • 13
  • 8
  • 5
  • 3
  • 3
  • 3
  • 2
  • 1
ELISA, Western Blotting (WB)
  • Épitope

    • 15
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 752-1974

    Fonction

    Anti-MED12 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins

    Attributs du produit

    Anti-MED12 Antibody Picoband® (ABIN7602421). 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.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human MED12 recombinant protein (Position: Q752-Q1974).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.25-0.5 μg/mL, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Barbieri, C. E., Baca, S. C., Lawrence, M. S., Demichelis, F., Blattner, M., Theurillat, J.-P., White, T. A., Stojanov, P., Van Allen, E., Stransky, N., Nickerson, E., Chae, S.-S., and 34 others. Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer. Nature Genet. 44: 685-689, 2012. 2. Beyer, K. S., Klauck, S. M., Benner, A., Poustka, F., Poustka, A. Association studies of the HOPA dodecamer duplication variant in different subtypes of autism. Am. J. Med. Genet. 114: 110-115, 2002. 3. Cools, F., Jaeken, J. Hardikar syndrome: a new syndrome with cleft lip/palate, pigmentary retinopathy and cholestasis. Am. J. Med. Genet. 71: 472-474, 1997.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Concentration

    500 μg/mL

    Buffer

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.
  • Antigène

    MED12 (Mediator Complex Subunit 12 (MED12))

    Autre désignation

    MED12

    Sujet

    Synonyms: Protein argonaute-1,Argonaute1,hAgo1,Argonaute RISC catalytic component 1,Eukaryotic translation initiation factor 2C 1,eIF-2C 1,eIF2C 1,Putative RNA-binding protein Q99,AGO1,EIF2C1,

    Tissue Specificity: Detected in blood plasma (at protein level).

    Background: Mediator of RNA polymerase II transcription, subunit 12 homolog (S. cerevisiae), also known as MED12, is a human gene found on the X chromosome. The initiation of transcription is controlled in part by a large protein assembly known as the preinitiation complex. A component of this preinitiation complex is a 1.2 MDa protein aggregate called Mediator. This Mediator component binds with a CDK8 subcomplex which contains the protein encoded by this gene, mediator complex subunit 12 (MED12), along with MED13, CDK8 kinase, and cyclin C. The CDK8 subcomplex modulates Mediator-polymerase II interactions and thereby regulates transcription initiation and reinitation rates. The MED12 protein is essential for activating CDK8 kinase. Defects in this gene cause X-linked Opitz-Kaveggia syndrome, also known as FG syndrome, and Lujan-Fryns syndrome.

    Poids moléculaire

    260 kDa

    ID gène

    9968

    UniProt

    Q93074

    Pathways

    Intracellular Steroid Hormone Receptor Signaling Pathway, Nuclear Hormone Receptor Binding, Stem Cell Maintenance, Chromatin Binding, Regulation of Lipid Metabolism by PPARalpha, Tube Formation
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