RFESD antibody (AA 51-157) (AbBy Fluor® 594)

Catalog No. ABIN2805917

This anti-RFESD antibody is a Rabbit Polyclonal antibody detecting RFESD in WB, IF (cc) and IF (p). Suitable for Rat.

Quick Overview for RFESD antibody (AA 51-157) (AbBy Fluor® 594) (ABIN2805917)

Target: RFESD (Rieske (Fe-S) Domain Containing (RFESD))

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RFESD antibody is conjugated to AbBy Fluor® 594

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-RFESD Antibody (AbBy Fluor® 594)

Binding Specificity: AA 51-157

Cross-Reactivity: Rat

Predicted Reactivity: Human,Mouse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human RFESD

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for RFESD

Target: RFESD (Rieske (Fe-S) Domain Containing (RFESD))

Alternative Name: RFESD

Background:

Synonyms: Rieske Fe S domain containing, Rieske domain containing protein, RFESD_HUMAN.

Background: RFESD, also known as Rieske domain-containing protein, is a 157 amino acid protein that binds one 2Fe-2S cluster per subunit. Involved in metal ion binding, RFESD contains one Rieske domain. The RFESD gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 5q15. Chromosome 5 makes up approximately 6 % of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Gene ID: 317671