KBP Polyklonale Antilichaam, AbBy FluorTM 594 Vervoeging

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.

Hypothetical protein LOC26128; KBP; KBP_HUMAN; KIAA1279; K1-binding protein; TTC20; Uncharacterized protein KIAA1279.

26128

Q96EK5

Human

151-250/621

KBP

AbBy Fluor™ 594

KLH conjugated synthetic peptide derived from human KBP

WB, IF (IHC-P)

Purified by Protein A.

590nm/617nm

1µg/µl

WB (1:300-5000), IF (IHC-P) (1:50-200)

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

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

26128

Mouse, Rat, Horse