SLITRK1 antibody (AA 22-696)

Catalog No. ABIN7872334

The Rabbit Polyclonal anti-SLITRK1 antibody (ABIN7872334) specifically detects SLITRK1 in WB, ELISA and FACS. The antibody is reactive with Human samples.

Quick Overview for SLITRK1 antibody (AA 22-696) (ABIN7872334)

Target: SLITRK1 (SLIT and NTRK-Like Family, Member 1 (SLITRK1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLITRK1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Product Details anti-SLITRK1 Antibody

Binding Specificity: AA 22-696

Purpose: SLITRK1 Antibody / SLIT and NTRK-like protein 1

Purification: Antigen affinity chromatography

Immunogen: An E.coli-derived human recombinant protein (amino acids D22-D696) was used as the immunogen for the SLITRK1 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the SLITRK1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the SLITRK1 Antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for SLITRK1

Target: SLITRK1 (SLIT and NTRK-Like Family, Member 1 (SLITRK1))

Alternative Name: SLITRK1

Background: SLITRK1 (SLIT and NTRK-like family, member 1) is a human gene that codes for a transmembrane and signalling protein that is part of the SLITRK gene family, which is responsible for synapse regulation and presynaptic differentiation in the brain. This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. However, the protein encoded by this gene lacks the region of homology to neurotrophin receptors. This protein is thought to be involved in neurite outgrowth. Mutations in this gene may be associated with Tourette syndrome. Alternative splicing results in multiple transcript variants.

UniProt: Q96PX8