H1500-01A

HADH (hydroxyacyl-Coenzyme A dehydrogenase, HAD, HADH1, HADHSC, HCDH, HHF4, Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial precursor, L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain, M/SCHAD, Medium and short chain L-3-hydroxyacyl-coenzyme A dehydrogenase, MGC8392, SCHAD, Short chain 3-hydroxyacyl-CoA dehydrogenase, Short chain 3-hydroxyacyl-CoA dehydrogenase, mitochondrial precursor)

Size

£642.00

SKU:: H1500-01A
Purity:: Purified by affinity chromatography.
Storage Conditions:: -20°C
Supplier:: United States Biological
Host:: Goat
Immunogen:: Synthetic peptide, C-YERGDASKEDID, from the internal region of human HADH.
Format:: Supplied as a liquid in Tris saline, pH 7.3, 0.5% BSA, 0.02% sodium azide.
Extra Details:: Short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD; EC1.1.1.35) plays an essential role in the mitochondrial beta-oxidation of short chain fatty acids. It catalyzes the reversible dehydrogenation of 3-hydroxyacyl-CoAs to their corresponding 3-ketoacyl-CoAs with concomitant reduction of NAD to NADH and exerts it highest activity toward 3-hydroxybutyryl-CoA. Applications: Suitable for use in ELISA and Western Blot. Other applications not tested. Recommended Dilutions: ELISA: 1:64,000 Western Blot: 0.01-0.03ug/ml Optimal dilutions to be determined by the researcher. Positive Control: Human Heart, Muscle and Kidney lysates Storage and Stability: May be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot and store at -20°C. Aliquots are stable for at least 12 monthsat -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. Peptide Blocking: Corresponding peptide is available for Peptide Blocking studies. See H1500-01A-P. Antibody is typically 0.5mg/ml and peptide is supplied as a 100ul pellet. When peptide is reconstituted in 200ul water, the concentration would also be 0.5mg/ml. To start, the best ratio would be 1:1 (molar excess of peptide relative to antibody when identical volumes are mixed). Mix equal volumes of peptide and antibody at the required dilution and leave at ambient temperature. It is best is to have two identical blots to be incubated with equal amount of antibody, but one with the antibody pre-adsorbed to the peptide for 20min. Then incubate and develop the two blots in parallel.

Shipping Conditions:: Blue Ice