RFESD antibody (AA 51-157) (Biotin)

Catalog No. ABIN1399381

Product Details anti-RFESD Antibody (Biotin)

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

Binding Specificity: AA 51-157

Reactivity: Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RFESD antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

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: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Expiry Date: 12 months

Target Details for RFESD

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

Alternative Name: RFESD (RFESD Products)

Synonyms: MGC82457 antibody, zgc:112118 antibody, AI256775 antibody, D030068K09 antibody, RGD1308284 antibody, Rieske Fe-S domain containing antibody, Rieske (Fe-S) domain containing L homeolog antibody, Rieske (Fe-S) domain containing antibody, RFESD antibody, rfesd.L antibody, rfesd antibody, Rfesd antibody

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