AAMDC anticorps (Biotin)

N° du produit ABIN1405525

Détail du produit anti-AAMDC anticorps (Biotin)

Antigène: AAMDC (Adipogenesis Associated Mth938 Domain Containing (AAMDC))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AAMDC est conjugé à/à la Biotin

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C11ORF67/PTD015

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur AAMDC

Antigène: AAMDC (Adipogenesis Associated Mth938 Domain Containing (AAMDC))

Autre désignation: C11ORF67 (AAMDC Produits)

Synonymes: anticorps C11orf67, anticorps C29H11orf67, anticorps c11orf67, anticorps zgc:112239, anticorps CK067, anticorps RGD1561459, anticorps 1810020D17Rik, anticorps 1810037D19Rik, anticorps LI2, anticorps adipogenesis associated Mth938 domain containing, anticorps adipogenesis associated, Mth938 domain containing, anticorps AAMDC, anticorps aamdc, anticorps Aamdc

Sujet:

Synonyms: Chromosome 11 open reading frame 67, CK067, FLJ21035, Hypothetical protein LOC28971, MGC3367, PTD015, UPF0366 protein C11orf67, AAMDC_HUMAN.

Background: PTD015 is a 122 amino acid protein that belongs to the UPF0366 family. Existing as three alternatively spliced isoforms, the PTD015 gene is conserved in dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 11q14.1. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The PTD015 gene product has been provisionally designated PTD015 pending further characterization.

UniProt: Q9H7C9