FAM13C anticorps (AA 51-150)

N° du produit ABIN872966

L’anticorps anti-FAM13C Polyclonal Lapin est utilisé pour la détection de FAM13C dans des échantillons de Humain. Il a été validé pour WB, IF (cc), IF (p), IHC (fro) et IHC (p).

Aperçu rapide pour FAM13C anticorps (AA 51-150) (ABIN872966)

Antigène: FAM13C (Family with Sequence Similarity 13, Member C (FAM13C))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM13C est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-FAM13C anticorps

Épitope: AA 51-150

Fonction: FAM13C1 Polyclonal Antibody

Réactivité croisée: Humain, Souris, Rat

Homologie: Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM13C1

Isotype: IgG

Information d'application

Indications d'application: WB(1:300-5000),

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 FAM13C

Antigène: FAM13C (Family with Sequence Similarity 13, Member C (FAM13C))

Autre désignation: Fam13c1

Sujet:

Synonyms: Family with sequence similarity 13 member C1, family with sequence similarity 13, member C: Hypothetical protein LOC220965, MGC33233, RGD1310149, FA13C_HUMAN.

Background: FAM13C1, also known as FAM13C, is a 585 amino acid protein that belongs to the FAM13 family. Existing as three alternatively spliced isoforms, the gene encoding FAM13C1 maps to human chromosome 10, which contains over 800 genes, 135 million nucleotides and makes up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.

ID gène: 220965