SLC22A12 Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP2-97265

Novus Biologicals, part of Bio-Techne

Key Product Details

Species Reactivity

Human

Applications

Immunohistochemistry-Paraffin

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

View all SLC22A12 Antibodies »

Product Specifications

Immunogen

Produced in rabbits immunized with E. coli-derived Human SLC22A12 fragment.

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Description

This antibody can be stored at 2C to 8C for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20C to -80C. Avoid repeated freeze-thaw cycles.

Scientific Data Images for SLC22A12 Antibody

Immunohistochemistry-Paraffin: SLC22A12 Antibody [NBP2-97265]

Immunohistochemistry-Paraffin: SLC22A12 Antibody [NBP2-97265]

Immunohistochemistry-Paraffin: SLC22A12 Antibody [NBP2-97265] - Immunochemical staining of human SLC22A12 in human kidney with rabbit polyclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.

Applications for SLC22A12 Antibody

Application
Recommended Usage

Immunohistochemistry-Paraffin

1:100-1:500

Formulation, Preparation, and Storage

Purification

Antigen and protein A Affinity-purified

Formulation

PBS

Preservative

0.03% Proclin 300

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.

Background: SLC22A12

SLC22A12, also known as urate transporter 1 (URAT1), is a member of the organic cation/anion/zwitterion transporter family. This transporter is present on the epithelial cells of proximal tubules in the renal cortex and mediates urate uptake. Gene mutations or functional defects of URAT1 have been identified in patients with renal hypouricemia, which is characterized by low serum urate levels. Disorders associated with this condition include uric acid urolithiasis; hematuria; hypercalcemia; or occasionally, exercise-induced acute renal failure.

Long Name

Solute carrier family 22 member 12

Alternate Names

OATL4, RST, UNQ6453/PRO34004, URAT1

Gene Symbol

SLC22A12

Additional SLC22A12 Products

Product Documents for SLC22A12 Antibody

Product Datasheets

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for SLC22A12 Antibody

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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