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BBS10 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-BBS10 a été validé pour WB et FACS. Il convient pour détecter BBS10 dans des échantillons de Humain.
N° du produit ABIN651074

Aperçu rapide pour BBS10 anticorps (C-Term) (ABIN651074)

Antigène

Voir toutes BBS10 Anticorps
BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

Reactivité

  • 41
  • 2
  • 1
  • 1
Humain

Hôte

  • 40
  • 1
Lapin

Clonalité

  • 41
Polyclonal

Conjugué

  • 13
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp BBS10 est non-conjugé

Application

  • 31
  • 15
  • 13
  • 13
  • 8
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB24715
  • Épitope

    • 15
    • 7
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 515-544, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This BBS10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 515-544 amino acids from the C-terminal region of human BBS10.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Date de péremption

    6 months
  • Antigène

    BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

    Autre désignation

    BBS10

    Sujet

    BBS10 is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes.

    Poids moléculaire

    80838

    ID gène

    79738

    NCBI Accession

    NP_078961

    UniProt

    Q8TAM1
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