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Anti-TRAPPC2 / SEDL Antibody (aa7-56) LS-C170213

Catalog Size Price
LS-C170213-50 50 µg (1 mg/ml) Unavailable

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22 TRAPPC2 / SEDL Antibodies

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100% Guaranteed
Rabbit Polyclonal to Rat TRAPPC2 / SEDL
Rat, Human, Mouse, Chicken
Western blot (applications tested for the base form of this product only)


Rat, Human, Mouse, Chicken (tested or 100% immunogen sequence identity)
Unconjugated. Also available conjugated with Biotin, FITC, HRP.
Immunoaffinity purified


  • Western blot
  • (applications tested for the base form of this product only)

Specificity and Use

TRAPPC2 / SEDL antibody was raised against synthetic peptide located between aa7-56 of rat Trappc2 (Q5BJL8, NP_001020136). Percent identity by BLAST analysis: Mouse, Rat, Chicken (100%).
LS-E18256 - Lyophilized - 100 µg - $145.00
Immunizing peptide used to generate LS-C170213. Useful for pre-absorption and neutralization of the antibody's antigen binding site.


Lyophilized from PBS
50 µl Distilled water
Long term: -20°C, the use of 50% glycerol is recommended if storing aliquots in -20°C for long term use (up to 1 year); Short term (less than one week): +4°C. Avoid repeat freeze-thaw cycles.
For research use only.


O14582 NM_014563 NP_055378.1

TRAPPC2 Antibody, MIP-2a Antibody, SEDT Antibody, TRS20 Antibody, TRAPPC2P1 Antibody, ZNF547L Antibody, HYP38334 Antibody, MIP2A Antibody, SEDL Antibody, Sedlin Antibody

TRAPPC2 / SEDL is thought to be part of a large multi-subunit complex involved in the targeting and fusion of endoplasmic reticulum-to-Golgi transport vesicles with their acceptor compartment. In addition, the encoded protein can bind c-myc promoter-binding protein 1 and block its transcriptional repression capability. Mutations in this gene are a cause of spondyloepiphyseal dysplasia tarda (SEDT).

Western blot

Western blot
TRAPPC2 / SEDL antibody Western Blot of Trappc2 antibodies. Sample Tissue: Rat Stomach lysates. Antibody Dilution: 1.0 ug/ml.. This image was taken for the unconjugated form of this product. Other forms have not been tested.

Requested From: 
Date Requested: 3/20/2018

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