KIF1BP antibody (AA 180-220) (AbBy Fluor® 488)

Catalog No. ABIN1404256

Product Details anti-KIF1BP Antibody (AbBy Fluor® 488)

Target: KIF1BP (KIAA1279) (KIAA1279)

Binding Specificity: AA 180-220

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KIF1BP antibody is conjugated to AbBy Fluor® 488

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

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 (KIAA1279 Products)

Synonyms: KBP antibody, TTC20 antibody, 0710007C18Rik antibody, mKIAA1279 antibody, Kbp antibody, CPi-21 antibody, GHR-P63 antibody, Klkbp antibody, SPI-2 antibody, SPI-2.3 antibody, SPI2 antibody, Serpina3k antibody, Spin2 antibody, Spin2b antibody, Kiaa1279 antibody, KIAA1279 antibody, kbp antibody, KIF1 binding protein antibody, serine (or cysteine) proteinase inhibitor, clade A, member 3C antibody, KIF1BP antibody, Kif1bp antibody, Serpina3c antibody

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