Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

B9D1 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-B9D1 a été validé pour WB, IF et EIA. Il convient pour détecter B9D1 dans des échantillons de Humain.
N° du produit ABIN1450121

Aperçu rapide pour B9D1 anticorps (C-Term) (ABIN1450121)

Antigène

Voir toutes B9D1 Anticorps
B9D1 (B9 Protein Domain 1 (B9D1))

Reactivité

  • 9
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 8
  • 1
Lapin

Clonalité

  • 9
Polyclonal

Conjugué

  • 9
Cet anticorp B9D1 est non-conjugé

Application

  • 8
  • 6
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Enzyme Immunoassay (EIA)
  • Épitope

    • 3
    • 2
    • 1
    • 1
    • 1
    C-Term

    Purification

    Affinity chromatography purified via peptide column

    Immunogène

    18 amino acid synthetic peptide near the carboxy terminus of Human B9D1

    Isotype

    IgG
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    PBS containing 0.02 % Sodium Azide as preservative

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène

    B9D1 (B9 Protein Domain 1 (B9D1))

    Autre désignation

    B9D1

    Sujet

    Meckel syndrome (MKS) is an embryonic lethal, autosomal recessive disorder characterized by polycystic kidney disease, central nervous system defects, polydactyly and liver fibrosis. B9D1 is a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. B9D1, and its related protein B9D2, form a complex with MKS1, disruption of which causes MKS. B9D1 is thought to be required for normal hedgehog signaling, ciliogenesis, and ciliary protein localization .Synonyms: B9 domain-containing protein 1, EPPB9

    ID gène

    27077

    NCBI Accession

    NP_056496
Vous êtes ici:
Chat with us!