FUNDC1 anticorps (AA 51-150) (Cy5)

N° du produit ABIN1704898

Détail du produit anti-FUNDC1 anticorps (Cy5)

Antigène: FUNDC1 (FUN14 Domain Containing 1 (FUNDC1))

Épitope: AA 51-150

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FUNDC1 est conjugé à/à la Cy5

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

Réactivité croisée: Humain, Souris, Rat

Homologie: Dog,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FUNDC1

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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 FUNDC1

Antigène: FUNDC1 (FUN14 Domain Containing 1 (FUNDC1))

Autre désignation: Fundc1 (FUNDC1 Produits)

Synonymes: anticorps fundc1-a, anticorps 1500005J14Rik, anticorps 1810033P05Rik, anticorps zgc:92600, anticorps FUN14 domain-containing protein 1-like, anticorps FUN14 domain containing 1 S homeolog, anticorps FUN14 domain containing 1, anticorps LOC100357289, anticorps fundc1.S, anticorps FUNDC1, anticorps Fundc1, anticorps fundc1

Sujet:

Synonyms: FUN14 domain containing protein 1, FUN14 domain-containing protein 1, FUND1_HUMAN.

Background: FUNDC1 is a 155 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC1 maps to human chromosome Xp11.3 and mouse chromosome X A1.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

ID gène: 139341