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ATP2A1/SERCA1 anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement ATP2A1/SERCA1 dans WB, IHC et FACS. Il présente une réactivité avec des échantillons de Humain, Rat et Souris.
N° du produit ABIN3043792
500,50 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 8 à 12 jours ouvrables

Aperçu rapide pour ATP2A1/SERCA1 anticorps (N-Term) (ABIN3043792)

Antigène

Voir toutes ATP2A1/SERCA1 (ATP2A1) Anticorps
ATP2A1/SERCA1 (ATP2A1) (ATPase, Ca++ Transporting, Cardiac Muscle, Fast Twitch 1 (ATP2A1))

Reactivité

  • 53
  • 31
  • 24
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 63
  • 8
Lapin

Clonalité

  • 51
  • 20
Polyclonal

Conjugué

  • 36
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ATP2A1/SERCA1 est non-conjugé

Application

  • 56
  • 26
  • 22
  • 16
  • 14
  • 13
  • 13
  • 12
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
  • Épitope

    • 16
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-32, N-Term

    Fonction

    Anti-SERCA1 ATPase/ATP2A1 Antibody

    Séquence

    MEAAHAKTTE ECLAYFGVSE TTGLTPDQVK RN

    Réactivité croisée (Details)

    No cross-reactivity with other proteins

    Attributs du produit

    Anti-SERCA1 ATPase/ATP2A1 Antibody (ABIN3043792). Tested in IHC, WB applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

    Purification

    Immunogen affinity purified.

    Immunogène

    A synthetic peptide corresponding to a sequence at the N-terminus of human SERCA1 ATPase, different from the related mouse and rat sequences by three amino acids.

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.5 μg/mL, Mouse, Rat
    Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human, Rat
    Flow Cytometry(Fixed), 1-3 μg/1x106 cells, Human

    Commentaires

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB, supported by ABIN921231 in IHC(P).

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 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 and 0.2 mg Na2HPO4.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store 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 freeze-thaw cycles.
  • Antigène

    ATP2A1/SERCA1 (ATP2A1) (ATPase, Ca++ Transporting, Cardiac Muscle, Fast Twitch 1 (ATP2A1))

    Autre désignation

    ATP2A1

    Sujet

    Synonyms: Sarcoplasmic/endoplasmic reticulum calcium ATPase 1,SERCA1,SR Ca (2+)-ATPase 1,3.6.3.8,Calcium pump 1,Calcium-transporting ATPase sarcoplasmic reticulum type, fast twitch skeletal muscle isoform,Endoplasmic reticulum class 1/2 Ca (2+) ATPase,ATP2A1,

    Tissue Specificity: Skeletal muscle, fast twitch muscle (type II) fibers.

    Background: SERCA1, also called ATP2A1, is an enzyme that in humans is encoded by the ATP2A1 gene. This gene encodes one of the SERCA Ca (2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. The SERCA1 gene is mapped to 16p11.2. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction. It has been determined that the human SERCA1 gene is 26 kb long and contains 23 exons, of which can be alternatively spliced. Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing impairment of muscular relaxation during exercise.

    Poids moléculaire

    110 kDa

    ID gène

    487

    UniProt

    O14983

    Pathways

    Ribonucleoside Biosynthetic Process
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