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Fibrillin 2 anticorps (AA 2740-2912)

L’anticorps Lapin Polyclonal anti-Fibrillin 2 a été validé pour ELISA et WB. Il convient pour détecter Fibrillin 2 dans des échantillons de Humain.
N° du produit ABIN7601047

Aperçu rapide pour Fibrillin 2 anticorps (AA 2740-2912) (ABIN7601047)

Antigène

Voir toutes Fibrillin 2 (FBN2) Anticorps
Fibrillin 2 (FBN2)

Reactivité

  • 31
  • 8
  • 2
  • 1
  • 1
Humain

Hôte

  • 32
  • 3
  • 2
Lapin

Clonalité

  • 34
  • 3
Polyclonal

Conjugué

  • 17
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Fibrillin 2 est non-conjugé

Application

  • 16
  • 13
  • 13
  • 13
  • 9
  • 6
  • 6
  • 5
  • 3
  • 1
  • 1
ELISA, Western Blotting (WB)
  • Épitope

    • 15
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 2740-2912

    Fonction

    Anti-fibrillin 2/FBN2 Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-fibrillin 2/FBN2 Antibody Picoband® (ABIN7601047). 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 fibrillin 2/FBN2 recombinant protein (Position: N2740-Y2912).

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.25-0.5 μg/mL, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Babcock, D., Gasner, C., Francke, U., Maslen, C. A single mutation that results in an asp-to-his substitution and partial exon skipping in a family with congenital contractual arachnodactyly. Hum. Genet. 103: 22-28, 1998. 2. Belleh, S., Zhou, G., Wang, M., Der Kaloustian, V. M., Pagon, R. A., Godfrey, M. Two novel fibrillin-2 mutations in congenital contractural arachnodactyly. Am. J. Med. Genet. 92: 7-12, 2000. 3. Lee, B., Godfrey, M., Vitale, E., Hori, H., Mattei, M.-G., Sarfarazi, M., Tsipouras, P., Ramirez, F., Hollister, D. W. Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. Nature 352: 330-334, 1991.

    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

    Fibrillin 2 (FBN2)

    Autre désignation

    FBN2

    Sujet

    Synonyms: Vacuolar protein sorting-associated protein 4B, Cell migration-inducing gene 1 protein, Suppressor of K (+) transport growth defect 1, Protein SKD1, VPS4B, SKD1, VPS42, MIG1

    Tissue Specificity: Ubiquitously expressed.

    Background: Fibrillin is a glycoprotein, which is essential for the formation of elastic fibers found in connective tissue. The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly.

    Poids moléculaire

    315 kDa, 250 kDa

    ID gène

    2201

    UniProt

    P35556

    Pathways

    Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
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