MSANTD1 anticorps (AA 50-100) (FITC)

N° du produit ABIN1405862

L’anticorps Lapin Polyclonal anti-MSANTD1 a été validé pour WB et IF (p). Il convient pour détecter MSANTD1 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour MSANTD1 anticorps (AA 50-100) (FITC) (ABIN1405862)

Antigène: MSANTD1 (Myb/SANT-Like DNA-Binding Domain Containing 1 (MSANTD1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MSANTD1 est conjugé à/à la FITC

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-MSANTD1 anticorps (FITC)

Épitope: AA 50-100

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C4orf44

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur MSANTD1

Antigène: MSANTD1 (Myb/SANT-Like DNA-Binding Domain Containing 1 (MSANTD1))

Autre désignation: C4orf44

Sujet:

Synonyms: C4orf44, Myb/SANT-like DNA-binding domain-containing protein 1, MSANTD1

Background: Representing approximately 6 % of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf44 gene product has been provisionally designated C4orf44 pending further characterization.

ID gène: 345222

UniProt: Q6ZTZ1