SATL1 Antikörper (C-Term)

Produktnummer ABIN954676

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch SATL1 in WB und EIA. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für SATL1 Antikörper (C-Term) (ABIN954676)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SATL1 Antikörper ist unkonjugiert

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

Produktdetails anti-SATL1 Antikörper

Bindungsspezifität: AA 322-352, C-Term

Spezifität: Recognizes SATL1 (C-term)

Aufreinigung: Protein A column followed by peptide Affinity purification

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

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

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

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

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

Details zu SATL1

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

Andere Bezeichnung: SATL1

Hintergrund: 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

Gen-ID: 340562

NCBI Accession: NP_001012998