CCDC25 antibody (AA 71-170) (AbBy Fluor® 750)

Catalog No. ABIN4999241

Product Details anti-CCDC25 Antibody (AbBy Fluor® 750)

Target: CCDC25 (Coiled-Coil Domain Containing 25 (CCDC25))

Binding Specificity: AA 71-170

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC25 antibody is conjugated to AbBy Fluor® 750

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

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC25

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 CCDC25

Target: CCDC25 (Coiled-Coil Domain Containing 25 (CCDC25))

Alternative Name: CCDC25 (CCDC25 Products)

Synonyms: 2610528H13Rik antibody, NSrp70 antibody, RGD1307689 antibody, coiled-coil domain containing 25 antibody, CCDC25 antibody, Ccdc25 antibody

Background:

Synonyms: CCD25_HUMAN, CCDC25, coiled-coil domain containing 25, CCDC25 coiled coil domain containing 25.

Background: CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

Gene ID: 55246