SLAIN1 anticorps (AA 1-100) (Biotin)

N° du produit ABIN1700397

Cet anticorps anti-SLAIN1 est un anticorps Lapin Polyclonal détectant SLAIN1 dans ELISA, IHC (p) et IHC (fro). Adapté pour Humain.

Aperçu rapide pour SLAIN1 anticorps (AA 1-100) (Biotin) (ABIN1700397)

Antigène: SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLAIN1 est conjugé à/à la Biotin

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-SLAIN1 anticorps (Biotin)

Épitope: AA 1-100

Homologie: Human,Mouse,Rat,Dog,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SLAIN1/C13orf32

Isotype: IgG

Information d'application

Indications d'application: IHC-P 1:200-400
IHC-F 1:100-500

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 SLAIN1

Antigène: SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))

Autre désignation: SLAIN1

Sujet:

Synonyms: C13orf32, chromosome 13 open reading frame 32, FLJ30046, MGC131899, SLAI1_HUMAN, SLAIN mot family member 1, SLAIN mot family, member 1, SLAIN mot-containing protein 1, Slain1.

Background: SLAIN1 is a 561 amino acid member of the SLAIN motif-containing family and is expressed in embryonic stem cells, as well as in lung, brain and testis, where it exists as two alternatively spliced isoforms. The gene encoding SLAIN1 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4 % of the human genome. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.