TSACC/C1orf182 anticorps (AA 21-100) (AbBy Fluor® 350)

N° du produit ABIN1692617

Détail du produit anti-TSACC/C1orf182 anticorps (AbBy Fluor® 350)

Antigène: TSACC/C1orf182 (TSACC) (TSSK6 Activating Co-Chaperone (TSACC))

Épitope: AA 21-100

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TSACC/C1orf182 est conjugé à/à la AbBy Fluor® 350

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

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C1orf182

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 TSACC/C1orf182

Antigène: TSACC/C1orf182 (TSACC) (TSSK6 Activating Co-Chaperone (TSACC))

Autre désignation: C1orf182 (TSACC Produits)

Synonymes: anticorps SIP, anticorps TP53DINP1, anticorps TP53INP1A, anticorps TP53INP1B, anticorps Teap, anticorps p53DINP1, anticorps C1orf182, anticorps RP11-443G18.5, anticorps SSTK-IP, anticorps 1700021C14Rik, anticorps C3H1orf182, anticorps RGD1304953, anticorps tumor protein p53 inducible nuclear protein 1, anticorps TSSK6 activating cochaperone, anticorps TSSK6 activating co-chaperone, anticorps TP53INP1, anticorps TSACC, anticorps Tsacc

Sujet:

Synonyms: C1orf182, CA182_HUMAN, SSTK-interacting protein, SSTK-IP, Uncharacterized protein C1orf182.

Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf182 gene product has been provisionally designated C1orf182 pending further characterization.

ID gène: 128229