KIF1BP anticorps (AA 180-220) (Cy3)

N° du produit ABIN1422125

Détail du produit anti-KIF1BP anticorps (Cy3)

Antigène: KIF1BP (KIAA1279) (KIAA1279)

Épitope: AA 180-220

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KIF1BP est conjugé à/à la Cy3

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human KBP

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

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

Date de péremption: 12 months

Détails sur KIF1BP

Antigène: KIF1BP (KIAA1279) (KIAA1279)

Autre désignation: KBP (KIAA1279 Produits)

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

Sujet:

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.

ID gène: 26128

UniProt: Q96EK5