GDF6 anticorps (C-Term)

N° du produit ABIN391699

Cet anticorps Lapin Polyclonal détecte spécifiquement GDF6 dans WB, FACS et IHC (p). Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour GDF6 anticorps (C-Term) (ABIN391699)

Antigène: GDF6 (Growth Differentiation Factor 6 (GDF6))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GDF6 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB15615

Détail du produit anti-GDF6 anticorps

Épitope: AA 326-353, C-Term

Homologie: B, Rat

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Immunogène: This GDF6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 326-353 amino acids from the C-terminal region of human GDF6.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:10~50. FC: 1:10~50

Restrictions: For Research Use only

Stockage

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

Détails sur GDF6

Antigène: GDF6 (Growth Differentiation Factor 6 (GDF6))

Autre désignation: GDF6

Sujet: GDF6 is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily of secreted signaling molecules. This protein is required for normal formation of some bones and joints in the limbs, skull, and axial skeleton. Mutations in this protein result in colobomata, which are congenital abnormalities in ocular development, and in Klippel-Feil syndrome (KFS), which is a congenital disorder of spinal segmentation.

Poids moléculaire: 50662

ID gène: 392255

NCBI Accession: NP_001001557

UniProt: Q6KF10