FAM135B anticorps (AA 1080-1130) (Biotin)

N° du produit ABIN1400623

Détail du produit anti-FAM135B anticorps (Biotin)

Antigène: FAM135B (Family with Sequence Similarity 135, Member B (FAM135B))

Épitope: AA 1080-1130

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM135B est conjugé à/à la Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM135B

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

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 for 12 months.

Date de péremption: 12 months

Détails sur FAM135B

Antigène: FAM135B (Family with Sequence Similarity 135, Member B (FAM135B))

Autre désignation: FAM135B (FAM135B Produits)

Synonymes: anticorps MGC81353, anticorps C8ORFK32, anticorps RGD1308133, anticorps 1700010C24Rik, anticorps A830008O07Rik, anticorps family with sequence similarity 135 member B, anticorps family with sequence similarity 135 member B L homeolog, anticorps family with sequence similarity 135, member B, anticorps FAM135B, anticorps fam135b.L, anticorps Fam135b

Sujet:

Synonyms: C8ORFK32, Protein FAM135B, FAM135B

Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM135B gene product has been provisionally designated FAM135B pending further characterization.

ID gène: 51059

UniProt: Q49AJ0