FAM76B anticorps (Biotin)

N° du produit ABIN1403923

Détail du produit anti-FAM76B anticorps (Biotin)

Antigène: FAM76B (Family with Sequence Similarity 76, Member B (FAM76B))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM76B 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 FAM76B

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 FAM76B

Antigène: FAM76B (Family with Sequence Similarity 76, Member B (FAM76B))

Autre désignation: FAM76B (FAM76B Produits)

Synonymes: anticorps fa11h02, anticorps wu:fa11h02, anticorps zgc:73333, anticorps 2810485I05Rik, anticorps C78303, anticorps RGD1311077, anticorps family with sequence similarity 76 member B, anticorps family with sequence similarity 76, member B, anticorps family with sequence similarity 76 member B S homeolog, anticorps FAM76B, anticorps fam76b, anticorps fam76b.S, anticorps Fam76b

Sujet:

Synonyms: Family with sequence similarity 76 member B, Hypothetical protein LOC143684, MGC33371, FA76B_HUMAN.

Background: With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.

ID gène: 143684