SATL1 anticorps (C-Term)

N° du produit ABIN954676

Cet anticorps Lapin Polyclonal détecte spécifiquement SATL1 dans WB et EIA. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour SATL1 anticorps (C-Term) (ABIN954676)

Antigène: SATL1 (Spermidine/spermine N1-Acetyl Transferase-Like 1 (SATL1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SATL1 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-SATL1 anticorps

Épitope: AA 322-352, C-Term

Specificité: Recognizes SATL1 (C-term)

Purification: Protein A column followed by peptide Affinity purification

Immunogène: KLH conjugated synthetic peptide between 322-352 amino acids from the C-terminal region of Human SATL1 (NP_001012998.2) Genename: SATL1

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) Sodium Azide as preservative

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur SATL1

Antigène: SATL1 (Spermidine/spermine N1-Acetyl Transferase-Like 1 (SATL1))

Autre désignation: SATL1

Sujet: SATL1 (spermine N(1)-acetyltransferase-like protein 1) is a 508 amino acid protein that contains one N-acetyltransferase domain, and belongs to the acetyltransferase family. Existing as two alternatively spliced isoforms, the SATL1 gene is conserved in chimpanzee, dog, cow, mouse and rat, and maps to human chromosome Xq21.1. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.Synonyms: Spermidine/spermine N(1)-acetyltransferase-like protein 1

ID gène: 340562

NCBI Accession: NP_001012998