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ATTY Rabbit pAb
db22133
Datasheet
- Background This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible cognitive disability. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008]
- Immunogen A synthetic peptide of human ATTY
-
Gene ID
6898
-
Swiss Prot
P17735
- Synonyms TAT; Tyrosine aminotransferase
- Reactivity Human, Mouse, Rat
- Application WB, IHC, ICC/IF
-
Recommended dilution
WB: 1:1000
IHC: 1:20
ICC/IF: 1:20 - Calculated MW 50 kDa
- Observed MW 50 kDa
- Host species Rabbit
- Clonality Polyclonal
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Storage/Stability Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
订购信息
- Package Price (RMB)
- 20μL 598
- 50μL 998
- 100μL 1798
- 货期：现货
相关产品
For research use only. Not intended for diagnostic.
