KIF1BP antibody (AA 180-220) (FITC)

Catalog No. ABIN1404260

The Rabbit Polyclonal anti-KIF1BP antibody has been validated for WB and IF (p). It is suitable to detect KIF1BP in samples from Human, Mouse and Rat.

Quick Overview for KIF1BP antibody (AA 180-220) (FITC) (ABIN1404260)

Target: KIF1BP (KIAA1279) (KIAA1279)

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KIF1BP antibody is conjugated to FITC

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

Product Details anti-KIF1BP Antibody (FITC)

Binding Specificity: AA 180-220

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human KBP

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 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 KIF1BP

Target: KIF1BP (KIAA1279) (KIAA1279)

Alternative Name: KBP

Background:

Synonyms: Hypothetical protein LOC26128, KBP, KBP_HUMAN, KIAA1279, K1-binding protein, TTC20, Uncharacterized protein KIAA1279.

Background: Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.

Gene ID: 26128

UniProt: Q96EK5