C15orf40 anticorps

N° du produit ABIN7246064

Détail du produit anti-C15orf40 anticorps

Antigène: C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C15orf40 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Fusion protein of human C15orf40

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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.

Détails sur C15orf40

Antigène: C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

Autre désignation: C15orf40 (C15orf40 Produits)

Synonymes: anticorps MGC89060, anticorps AI851475, anticorps C15orf40, anticorps c15orf40, anticorps chromosome 15 open reading frame 40, anticorps RIKEN cDNA 3110040N11 gene, anticorps similar to RIKEN cDNA 3110040N11, anticorps chromosome 21 open reading frame, human C15orf40, anticorps chromosome 15 open reading frame 40 L homeolog, anticorps C15orf40, anticorps c15orf40, anticorps 3110040N11Rik, anticorps RGD1305713, anticorps C21H15orf40, anticorps c15orf40.L

Sujet: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf40 gene product has been provisionally designated C15orf40 pending further characterization.

Poids moléculaire:

Observed_MW: Refer to figures

Calculated_MW: 16 kDa

UniProt: Q8WUR7