![IHC-P analysis of human tonsil tissue using GTX34411 AMPD3 antibody [AMPD3/901]. IHC-P analysis of human tonsil tissue using GTX34411 AMPD3 antibody [AMPD3/901].](https://www.genetex.com/upload/website/prouct_img/normal/GTX34411/GTX34411_20200115_IHC-P_1260_w_23060801_300.webp)
IHC-P analysis of human tonsil tissue using GTX34411 AMPD3 antibody [AMPD3/901].
AMPD3 antibody [AMPD3/901]
GTX34411
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetAMPD3
Overview
- SupplierGeneTex
- Product NameAMPD3 antibody [AMPD3/901]
- Delivery Days Customer9
- Antibody SpecificityThis antibody recognizes a protein of ~90kDa, which is identified as Adenosine Monophosphate Deaminase, isoform E (AMPD3). It shows reactivity with cells of the erythroid lineage at all stages of maturation in the peripheral blood, bone marrow, and fetal
- Application Supplier NoteIHC-P: 2-4microg/ml for 30 minutes at RT. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDAMPD3/901
- Concentration0.2 mg/ml
- ConjugateUnconjugated
- Gene ID272
- Target nameAMPD3
- Target descriptionadenosine monophosphate deaminase 3
- Target synonymsadenosine monophosphate deaminase (isoform E); AMP aminohydrolase; AMP deaminase 3; erythrocyte AMP deaminase; erythrocyte type AMP deaminase; erythrocyte-specific AMP deaminase; myoadenylate deaminase
- HostMouse
- IsotypeIgG2b
- Protein IDQ01432
- Protein NameAMP deaminase 3
- Scientific DescriptionThis gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203