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HGD, Mouse, Clone: 1F1, Abnova™

Mouse monoclonal antibody raised against a full-length recombinant HGD.

Supplier:  Abnova Corporation H00003081M11

Catalog No. 89-022-475


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Description

Description

Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26. [provided by RefSeq

Sequence: MAELKYISGFGNECSSEDPRCPGSLPEGQNNPQVCPYNLYAEQLSGSAFTCPRSTNKRSWLYRILPSVSHKPFESIDEGHVTHNWDEVDPDPNQLRWKPFEIPKASQKKVDFVSGLHTLCGAGDIKSNNGLAIHIFLCNTSMENRCFYNSDGDFLIVPQKGNLLIYTEFGKMLVQPNEICVIQRGMRFSIDVFEETRGYILEVYGVHLELPDLGPIGANGLANPRDFLIPIAWYEDRQVPGGYTVINKYQGKLFAAKQDVSPFNVVAWHGNYTPYKYNLKNFMVINSVAFDHADPSIFTVLTALRRPARSSWHLRGLPMAPWHLCLNHL
Specifications

Specifications

HGD
Monoclonal
Unconjugated
PBS with no preservative; pH 7.4
BC020792
HGD
HGD (AAH20792, 1 a.a. ∼ 329 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
100 μg
Primary
Human
Antibody
IgG2a κ
ELISA, Immunoprecipitation, Western Blot
1F1
Mouse monoclonal antibody raised against a full-length recombinant HGD.
HGD
AKU/HGO
Mouse
Affinity chromatography
RUO
3081
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
Liquid
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