HAL Antilichaam

Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids. Several transcript variants encoding different isoforms have been found for this gene.

3034

P42357

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-200 of human HAL (NP_002099.1) .

Unconjugated

Primary Antibodies

Signal Transduction

Affinity purification

Mouse liver

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 73kDa

IgG

HAL

Rat liver

Histidine ammonia-lyase

Homo sapiens

HAL, HIS, HSTD, histidase

WB, IHC, IF

Liquid