CTTNBP2NL antibody (AA 5-110) (Alexa Fluor 555)

Catalog No. ABIN6942711

Product Details anti-CTTNBP2NL Antibody (Alexa Fluor 555)

Target: CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))

Binding Specificity: AA 5-110

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CTTNBP2NL antibody is conjugated to Alexa Fluor 555

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

Cross-Reactivity: Rat

Predicted Reactivity: Human,Mouse,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CTTNBP2NL

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 CTTNBP2NL

Target: CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))

Alternative Name: CTTNBP2NL (CTTNBP2NL Products)

Synonyms: AA552995 antibody, AA589392 antibody, AU018624 antibody, BC003236 antibody, mKIAA1433 antibody, CTTNBP2 N-terminal like antibody, CTTNBP2NL antibody, Cttnbp2nl antibody

Background:

Synonyms: CT2NL_HUMAN, CTTNBP2 N terminal like, CTTNBP2 N terminal like protein, CTTNBP2 N-terminal-like protein, Cttnbp2nl, DKFZp547A023, FLJ13278, KIAA1433.

Background: CTTNBP2NL is a 639 amino acid protein that is encoded by a gene that maps to human chromosome 1p13.2. 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.

Gene ID: 55917

UniProt: Q9P2B4