Thermo Fisher Scientific HGD Polyclonal Antibody
Human HGD 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB 및 ELISA에 검증됨. 고순도 Affinity Chromatography 정제. PBS/glycerol buffer에 보존되며 -20°C에서 보관. 연구용으로만 사용 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 1:500–1:2,000
ELISA
- Tested Dilution: 1 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 226–445 of human HGD (NP_0001782) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.72 mg/mL |
| Purification | Affinity Chromatography |
| Storage Buffer | PBS, pH 7.3, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Wet ice |
| RRID | AB_2806624 |
Product Specific Information
Immunogen sequence:
DFLIPIAWYE DRQVPGGYTV INKYQGKLFA AKQDVSPFNV VAWHGNYTPY KYNLKNFMVI NSVAFDHADP SIFTVLTAKS VRPGVAIADF VIFPPRWGVA DKTFRPPYYH RNCMSEFMGL IRGHYEAKQG GFLPGGGSLH STMTPHGPDA DCFEKASKVK LAPERIADGT MAFMFESSLS LAVTKWGLKA SRCLDENYHK CWEPLKSHFT PNSRNPAEPNPositive Samples: SKOV3
Target Information
This gene encodes the enzyme homogentisate 1,2 dioxygenase, which is involved in the catabolism of the amino acids tyrosine and phenylalanine.
Mutations in this gene cause the autosomal recessive metabolic disorder alkaptonuria.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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