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SNX25 anticorps (AA 48-584)

Cet anticorps Lapin Polyclonal détecte spécifiquement SNX25 dans WB, ELISA et FACS. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7601838

Aperçu rapide pour SNX25 anticorps (AA 48-584) (ABIN7601838)

Antigène

Voir toutes SNX25 Anticorps
SNX25 (Sorting Nexin 25 (SNX25))

Reactivité

Humain, Souris, Rat

Hôte

  • 36
  • 3
Lapin

Clonalité

  • 37
  • 2
Polyclonal

Conjugué

  • 14
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SNX25 est non-conjugé

Application

  • 32
  • 15
  • 13
  • 13
  • 8
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 15
    • 7
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 48-584

    Fonction

    Anti-SNX25 Antibody Picoband®

    Attributs du produit

    Anti-SNX25 Antibody Picoband® (ABIN7601838). Tested in WB, Flow Cytometry, ELISA 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 SNX25 recombinant protein (Position: H48-K584). Human SNX25 shares 86.4% amino acid (aa) sequence identity with mouse SNX25.
  • Indications d'application

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Chance, P. F., Rabin, B. A., Ryan, S. G., Ding, Y., Scavina, M., Crain, B., Griffin, J. W., Cornblath, D. R. Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34. Am. J. Hum. Genet. 62: 633-640, 1998. 2. Dyck, P. J., Lambert, E. H. Lower motor and primary sensory neuron disease with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations. Arch. Neurol. 18: 619-625, 1968. 3. Gemignani, F., Guidetti, D., Bizzi, P., Preda, P., Cenacchi, G., Marbini, A. Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous: report of nerve biopsy in four cases and review of the literature. Acta Neuropath. 83: 196-201, 1992.

    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

    SNX25 (Sorting Nexin 25 (SNX25))

    Autre désignation

    SNX25

    Sujet

    SNX25 (sorting nexin 25), also known as SBBI31 or MSTP043, is an 840 amino acid protein suggested to function in several stages of intracellular trafficking. A member of the sorting nexin family, SNX25 contains one PX (phox homology) domain, an RGS domain and one PXA domain. May be involved in several stages of intracellular trafficking.

    Poids moléculaire

    100 kDa

    ID gène

    83891

    UniProt

    Q9H3E2

    Pathways

    Regulation of G-Protein Coupled Receptor Protein Signaling
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