FAM207A anticorps (AA 95-120)

N° du produit ABIN1385685

Cet anticorps anti-FAM207A Polyclonal Lapin (ABIN1385685) détecte spécifiquement FAM207A dans IHC (p), IHC (fro) et IF. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour FAM207A anticorps (AA 95-120) (ABIN1385685)

Antigène: FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM207A est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (IF)

Détail du produit anti-FAM207A anticorps

Épitope: AA 95-120

Fonction: C21orf70 Polyclonal Antibody

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C21orf70

Isotype: IgG

Information d'application

Indications d'application: IHC-P(1:300-5000), IHC-F(1:200-400), IF(1:50-200)

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur FAM207A

Antigène: FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))

Autre désignation: C21orf70

Sujet:

Synonyms: Chromosome 21 open reading frame 70, CU070_HUMAN, Hypothetical protein LOC85395, PRED56, Uncharacterized protein C21orf70.

Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.

ID gène: 85395

UniProt: Q9NSI2