SATL1 antibody (C-Term)

Catalog No. ABIN954676

This Rabbit Polyclonal antibody specifically detects SATL1 in WB and EIA. It exhibits reactivity toward Human.

Quick Overview for SATL1 antibody (C-Term) (ABIN954676)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SATL1 antibody is un-conjugated

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

Product Details anti-SATL1 Antibody

Binding Specificity: AA 322-352, C-Term

Specificity: Recognizes SATL1 (C-term)

Purification: 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

Isotype: Ig Fraction

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.25 mg/mL

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

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

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

Target Details for SATL1

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

Alternative Name: SATL1

Background: 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

Gene ID: 340562

NCBI Accession: NP_001012998