HMBS Polyklonale Antilichaam
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP) . AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
HEM3_HUMAN; HMBS; Hydroxymethylbilane synthase; PBG D; PBG-D; PBGD; Porphobilinogen deaminase; Pre uroporphyrinogen synthase; Pre-uroporphyrinogen synthase; UPS; Uroporphyrinogen I synthase; Uroporphyrinogen I synthetase.
3145
• Rabbit
Human, Mouse, Rat
21-120/361
HMBS
• Polyclonal
• IgG
Unconjugated
KLH conjugated synthetic peptide derived from human HMBS/PBGD
ELISA, IHC-P, IHC-F, IF
Purified by Protein A.
1µg/µl
ELISA (ELISA=1:5000-10000), IHC-P (IHC-P=1:100-500), IHC-F (IHC-F=1:100-500), IF (IF=1:50-200)
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Unmodified
Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
3145
Beschrijving
HMBS Polyklonale Antilichaam Beschikbaar in 100 µL. Bestel eenvoudig online met snelle levering.
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