SVOPL antibody (AA 241-269)

Catalog No. ABIN1538165

Product Details anti-SVOPL Antibody

Target: SVOPL (SVOP-Like (SVOPL))

Binding Specificity: AA 241-269

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SVOPL antibody is un-conjugated

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This SVOPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 241-269 amino acids from the Central region of human SVOPL.

Clone: RB35924

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 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.

Storage: 4 °C,-20 °C

Storage Comment: SVOPL Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Expiry Date: 6 months

Target Details for SVOPL

Target: SVOPL (SVOP-Like (SVOPL))

Alternative Name: SVOPL (SVOPL Products)

Synonyms: zgc:101741 antibody, 9430071P14Rik antibody, SVOP like antibody, SVOP-like antibody, SV2 related protein homolog (rat)-like antibody, SVOPL antibody, svopl antibody, Svopl antibody

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.

Molecular Weight: 53991

Gene ID: 136306

NCBI Accession: NP_001132928, NP_777619

UniProt: Q8N434