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Dynactin 1 anticorps (AA 1042-1278)

Cet anticorps anti-Dynactin 1 est un anticorps Lapin Polyclonal détectant Dynactin 1 dans WB, ELISA, IHC, IF, ICC et FACS. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7599660

Aperçu rapide pour Dynactin 1 anticorps (AA 1042-1278) (ABIN7599660)

Antigène

Voir toutes Dynactin 1 (DCTN1) Anticorps
Dynactin 1 (DCTN1)

Reactivité

  • 56
  • 22
  • 16
  • 5
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  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
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Humain, Souris, Rat

Hôte

  • 39
  • 14
  • 3
  • 1
Lapin

Clonalité

  • 43
  • 14
Polyclonal

Conjugué

  • 36
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  • 1
  • 1
  • 1
  • 1
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  • 1
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Cet anticorp Dynactin 1 est non-conjugé

Application

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  • 1
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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunocytochemistry (ICC), Flow Cytometry (FACS)
  • Épitope

    • 15
    • 5
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    • 2
    • 2
    • 2
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    • 1
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    AA 1042-1278

    Fonction

    Anti-DCTN1/p150-glued Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-DCTN1/p150-glued Antibody Picoband® (ABIN7599660). Tested in ELISA, Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human, Mouse, Rat. 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 DCTN1/p150-glued recombinant protein (Position: K1042-S1278).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.25 μg/mL, Human, Mouse, Rat
    Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Caroppo, P., Le Ber, I., Clot, F., Rivaud-Pechoux, S., Camuzat, A., De Septenville, A., Boutoleau-Bretonniere, C., Mourlon, V., Sauvee, M., Lebouvier, T., Bonnet, A.-M., Levy, R., Vercelletto, M., Brice, A. DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypes. JAMA Neurol. 71: 208-215, 2014. 2. Collin, G. B., Nishina, P. M., Marshall, J. D., Naggert, J. K. Human DCTN1: genomic structure and evaluation as a candidate for Alstrom syndrome. Genomics 53: 359-364, 1998. 3. Eaton, B. A., Fetter, R. D., Davis, G. W. Dynactin is necessary for synapse stabilization. Neuron 34: 729-741, 2002.

    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, 0.2 mg Na2HPO4.

    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

    Dynactin 1 (DCTN1)

    Autre désignation

    DCTN1

    Sujet

    Synonyms: Probetacellulin, Betacellulin, BTC, BTC

    Tissue Specificity: Highly expressed in testis.

    Background: Dynactin subunit 1 is a protein that in humans is encoded by the DCTN1 gene. This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. Dynactin is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit interacts with dynein intermediate chain by its domains ly binding to dynein and binds to microtubules via a highly conserved glycine-rich cytoskeleton-associated protein (CAP-Gly) domain in its N-terminus. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA).

    Poids moléculaire

    150 kDa

    ID gène

    1639

    UniProt

    Q14203

    Pathways

    M Phase, ER-Nucleus Signaling
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