HIBCH Mouse Monoclonal Antibody [Kloon ID: LBI3D11]

This gene encodes the enzyme responsible for hydrolysis of both HIBYL-CoA and beta-hydroxypropionyl-CoA. Mutations in this gene have been associated with 3-hyroxyisobutyryl-CoA hydrolase deficiency. Alternative splicing results in multiple transcript variants.

Carrier-free (BSA/glycerol-free) HIBCH mouse monoclonal antibody, clone LBI3D11

HIBYLCOAH

Homo sapiens 3-hydroxyisobutyryl-CoA hydrolase (HIBCH), transcript variant 1, mRNA; nuclear gene for mitochondrial product.

26275

Q6NVY1

Unconjugated

Beta-Alanine metabolism, Metabolic pathways, Propanoate metabolism, Valine, leucine and isoleucine degradation

Beta-Alanine metabolism, Metabolic pathways, Propanoate metabolism, Valine, leucine and isoleucine degradation

WB 1:500~2000, IF 1:100, FLOW 1:100

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

HIBCH

https://www.ncbi.nlm.nih.gov/gene/?term=26275

https://www.uniprot.org/uniprot/Q6NVY1