FAM160B1 anticorps (AA 521-630) (Alexa Fluor 750)

N° du produit ABIN5002378

Détail du produit anti-FAM160B1 anticorps (Alexa Fluor 750)

Antigène: FAM160B1 (Family with Sequence Similarity 160, Member B1 (FAM160B1))

Épitope: AA 521-630

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM160B1 est conjugé à/à la Alexa Fluor 750

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

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM160B1

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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 FAM160B1

Antigène: FAM160B1 (Family with Sequence Similarity 160, Member B1 (FAM160B1))

Autre désignation: FAM160B1 (FAM160B1 Produits)

Synonymes: anticorps zgc:162264, anticorps kiaa1600, anticorps KIAA1600, anticorps bA106M7.3, anticorps AI450540, anticorps mKIAA1600, anticorps RGD1306116, anticorps family with sequence similarity 160, member B1, anticorps family with sequence similarity 160 member B1, anticorps family with sequence similarity 160 member B1 S homeolog, anticorps fam160b1, anticorps FAM160B1, anticorps Fam160b1, anticorps fam160b1.S

Sujet:

Synonyms: DKFZp686D10123, F16B1_HUMAN, Fam160b1, Family with sequence similarity 160 member B1, Hypothetical protein LOC57700, KIAA1600, Protein FAM160B1.

Background: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which 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.