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SNX25 Antikörper (AA 48-584)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch SNX25 in WB, ELISA und FACS. Er zeigt eine Reaktivität gegenüber Human, Maus und Ratte.
Produktnummer ABIN7601838

Kurzübersicht für SNX25 Antikörper (AA 48-584) (ABIN7601838)

Target

Alle SNX25 Antikörper anzeigen
SNX25 (Sorting Nexin 25 (SNX25))

Reaktivität

Human, Maus, Ratte

Wirt

  • 36
  • 3
Kaninchen

Klonalität

  • 37
  • 2
Polyklonal

Konjugat

  • 14
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser SNX25 Antikörper ist unkonjugiert

Applikation

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

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

    Verwendungszweck

    Anti-SNX25 Antibody Picoband®

    Produktmerkmale

    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.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human SNX25 recombinant protein (Position: H48-K584). Human SNX25 shares 86.4% amino acid (aa) sequence identity with mouse SNX25.
  • Applikationshinweise

    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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Konzentration

    500 μg/mL

    Buffer

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    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.
  • Target

    SNX25 (Sorting Nexin 25 (SNX25))

    Andere Bezeichnung

    SNX25

    Hintergrund

    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.

    Molekulargewicht

    100 kDa

    Gen-ID

    83891

    UniProt

    Q9H3E2

    Pathways

    Regulation of G-Protein Coupled Receptor Protein Signaling
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