SVOPL antibody (Middle Region)

Catalog No. ABIN955017

The Rabbit Polyclonal anti-SVOPL antibody (ABIN955017) specifically detects SVOPL in WB and EIA. The antibody is reactive with Human samples.

Quick Overview for SVOPL antibody (Middle Region) (ABIN955017)

Target: SVOPL (SVOP-Like (SVOPL))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SVOPL antibody is un-conjugated

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

Product Details anti-SVOPL Antibody

Binding Specificity: AA 240-269, Middle Region

Specificity: This antibody detects SVOPL (Center).

Cross-Reactivity (Details): Species reactivity (tested):Human

Purification: Protein A column followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 240-269 amino acids from the Central region of human SVOPL

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, 0.09 % (W/V) sodium azide

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 at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.

Target Details for SVOPL

Target: SVOPL (SVOP-Like (SVOPL))

Alternative Name: SVOPL

Background: SVOPL (putative transporter SVOPL), also known as SV2-related protein-like, is a 492 amino acid multi-pass membrane protein belonging to the major facilitator superfamily. SVOPL is a paralog to synaptic vesicle protein (SVOP) that exists as two alternatively spliced isoforms. The gene encoding SVOPL maps to human chromosome 7q34. Chromosome 7 is approximately 158 milllion bases long, encodes over 1,000 genes and makes up approximately 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Deletions of portions of the q arm of chromosome 7 are linked to myeloid disorders, including acute myelogenous leukemia and myelodysplasia.Synonyms: Putative transporter

Molecular Weight: Molecular Weight: 53991 Da

Gene ID: 136306

NCBI Accession: NP_001132928