FAM98A anticorps (AA 251-350) (Alexa Fluor 750)

N° du produit ABIN5002442

Détail du produit anti-FAM98A anticorps (Alexa Fluor 750)

Antigène: FAM98A (Family with Sequence Similarity 98, Member A (FAM98A))

Épitope: AA 251-350

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM98A est conjugé à/à la Alexa Fluor 750

Application: Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Humain, Souris

Homologie: Rat,Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM98A

Isotype: IgG

Information d'application

Indications d'application: FCM 1:20-100
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 FAM98A

Antigène: FAM98A (Family with Sequence Similarity 98, Member A (FAM98A))

Autre désignation: FAM98A (FAM98A Produits)

Synonymes: anticorps 2810405J04Rik, anticorps AL024114, anticorps RGD1305486, anticorps family with sequence similarity 98 member A, anticorps family with sequence similarity 98, member A, anticorps FAM98A, anticorps Fam98a

Sujet:

Synonyms: FAM 98A, Family with sequence similarity 98 member A, Hypothetical protein LOC25940, LOC25940, Protein FAM98A, FA98A_HUMAN.

Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.

ID gène: 25940

Pathways: SARS-CoV-2 Protein Interactome