LOR antibody

Catalog No. ABIN2462467

Product Details anti-LOR Antibody

Target: LOR (Loricrin (LOR))

Reactivity: Please inquire

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LOR antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Purification: Antibody is purified by protein A chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LOR.

Application Details

Application Notes: LOR antibody can be used for detection of LOR by ELISA at 1:62500. LOR antibody can be used for detection of LOR by western blot at 5.0 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store LOR antibody at -20 °C.

Target Details for LOR

Target: LOR (Loricrin (LOR))

Alternative Name: LOR (LOR Products)

Synonyms: AI036317 antibody, S77319 antibody, RGD1559993 antibody, LOR antibody, loricrin antibody, Loricrin antibody, LOR antibody, Lor antibody, TVAG_146950 antibody, TVAG_228830 antibody, TVAG_228920 antibody, TVAG_238290 antibody, TVAG_035050 antibody, TVAG_070680 antibody, Bm1_52290 antibody, LOC100281109 antibody, LOC100281170 antibody

Target Type: Chemical

Background: LOR is a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.LOR encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in LOR may be the cause of both Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.

Molecular Weight: 35 kDa

Gene ID: 4014

NCBI Accession: NP_000418

UniProt: P23490