SAPCD2 anticorps (AA 301-394) (FITC)

N° du produit ABIN1709694

Cet anticorps anti-SAPCD2 est un anticorps Lapin Polyclonal détectant SAPCD2 dans WB, IF (cc) et IF (p). Adapté pour Rat.

Aperçu rapide pour SAPCD2 anticorps (AA 301-394) (FITC) (ABIN1709694)

Antigène: SAPCD2 (Suppressor APC Domain Containing 2 (SAPCD2))

Reactivité: Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SAPCD2 est conjugé à/à la FITC

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

Détail du produit anti-SAPCD2 anticorps (FITC)

Épitope: AA 301-394

Réactivité croisée: Rat

Homologie: Human,Mouse,Cow,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C9orf140

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 SAPCD2

Antigène: SAPCD2 (Suppressor APC Domain Containing 2 (SAPCD2))

Autre désignation: C9orf140

Sujet:

Synonyms: 2010317E24Rik, C9orf140, Chromosome 9 open reading frame 140, SAPC2_HUMAN, p42.3, Protein C9orf140, SAPCD2, Suppressor APC domain containing 2, Suppressor APC domain containing protein 2, TS/MDEP, Tumor specicity and mitosis phase-dependent expression protein.

Background: C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

ID gène: 89958