FAM36A anticorps (AA 51-118) (Alexa Fluor 594)

N° du produit ABIN2813081

Détail du produit anti-FAM36A anticorps (Alexa Fluor 594)

Antigène: FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))

Épitope: AA 51-118

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM36A est conjugé à/à la Alexa Fluor 594

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

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM36A

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 FAM36A

Antigène: FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))

Autre désignation: FAM36A (FAM36A Produits)

Synonymes: anticorps FAM36A, anticorps 2310005N03Rik, anticorps Fam36a, anticorps RGD1309105, anticorps cox20, anticorps fam36a, anticorps COX20, cytochrome c oxidase assembly factor, anticorps COX20 Cox2 chaperone, anticorps COX20 cytochrome C oxidase assembly factor, anticorps COX20 cytochrome c oxidase assembly factor L homeolog, anticorps COX20, anticorps Cox20, anticorps cox20.L

Sujet:

Synonyms: FAM 36A, Family with sequence similarity 36 member A, FLJ43269, Hypothetical protein LOC116228, OTTHUMP00000038200, Protein FAM36A.

Background: FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM36A gene product has been provisionally designated FAM36A pending further characterization.

ID gène: 116228