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RIN2 anticorps

Cet anticorps anti-RIN2 est un anticorps Lapin Polyclonal détectant RIN2 dans WB. Adapté pour Humain et Souris.
N° du produit ABIN6568165

Aperçu rapide pour RIN2 anticorps (ABIN6568165)

Antigène

Voir toutes RIN2 Anticorps
RIN2 (Ras and Rab Interactor 2 (RIN2))

Reactivité

  • 9
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Humain, Souris

Hôte

  • 5
  • 4
Lapin

Clonalité

  • 6
  • 3
Polyclonal

Conjugué

  • 9
Cet anticorp RIN2 est non-conjugé

Application

  • 9
  • 5
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Purification

    Affinity purification

    Immunogène

    Recombinant protein of human RIN2

    Isotype

    IgG
  • Indications d'application

    WB 1:500 - 1:2000

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    RIN2 (Ras and Rab Interactor 2 (RIN2))

    Autre désignation

    RIN2

    Sujet

    Synonyms: MACS ,RAB5 interacting protein 2,Ras and Rab interactor 2,RAS association (RalGDS/AF-6) domain containing protein JC265,Ras association domain family 4,Ras inhibitor JC265,Ras interaction/interference protein 2,RASSF4,RIN 2,RIN2,RIN2

    Background: The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants.

    Poids moléculaire

    Observed_MW: 120kDa

    Calculated_MW: 100kDa/105kDa

    ID gène

    54453

    UniProt

    Q8WYP3
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