![PAH antibody [N1C2]](https://www.genetex.com/upload/website/prouct_img/normal/GTX101290/GTX101290_43712_20190920_WB_TPM_watermark_w_23060100_725.webp)
![PAH antibody [N1C2]](https://www.genetex.com/upload/website/prouct_img/normal/GTX101290/GTX101290_43712_20200806_ICC_IF_w_23060100_578.webp)
GTX101290
PAH antibody [N1C2]
Cannot supply to this region.
- SKU:
- GTX101290
- Additional Names:
- phenylalanine hydroxylase , PH , PKU , PKU1
- Application:
- WB, IF, ICC
- Concentration:
- 1.76 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 20% Glycerol, 0.025% ProClin 300.
- Immunogen:
- Recombinant protein encompassing a sequence within the center region of human PAH. The exact sequence is proprietary.
- Clone:
- N1C2
- Uniprot:
- P00439
- Synonyms:
- PH;phe-4-monooxygenase;phenylalanine 4-monooxygenase;phenylalanine-4-hydroxylase;PKU;PKU1
- Extra Details:
- This gene encodes a member of the biopterin-dependent aromatic amino acid hydroxylase protein family. The encoded phenylalanine hydroxylase enzyme hydroxylates phenylalanine to tyrosine and is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Aug 2017]
- Shipping Conditions:
- Blue Ice