C1orf177 antibody (AA 21-100) (AbBy Fluor® 680)

Catalog No. ABIN4998077

This anti-C1orf177 antibody is a Rabbit Polyclonal antibody detecting C1orf177 in IF (p) and IF (cc). Suitable for Human.

Quick Overview for C1orf177 antibody (AA 21-100) (AbBy Fluor® 680) (ABIN4998077)

Target: C1orf177 (C1ORF177) (Chromosome 1 Open Reading Frame 177 (C1ORF177))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C1orf177 antibody is conjugated to AbBy Fluor® 680

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

Product Details anti-C1orf177 Antibody (AbBy Fluor® 680)

Binding Specificity: AA 21-100

Predicted Reactivity: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf177

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for C1orf177

Target: C1orf177 (C1ORF177) (Chromosome 1 Open Reading Frame 177 (C1ORF177))

Alternative Name: C1orf177

Background:

Synonyms: Chromosome 1 open reading frame 177, FLJ40201, Hypothetical protein LOC163747, Uncharacterized protein C1orf177, CA177_HUMAN.

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 C1orf177 gene product has been provisionally designated C1orf177 pending further characterization. There are two isoforms of C1orf177 that are produced as a result of alternative splicing events.

Gene ID: 163747