GOT1L1 (GeneName), Putative aspartate aminotransferase, cytoplasmic 2 (ProteinName), AATC2_HUMAN.
Product Name:
Human GOT1L1/ Putative aspartate aminotransferase, cytoplasmic 2 ELISA Kit
Cat.#:
E2107h
Brand:
EIAab®
Regulatory Status:
Alternative:
Glutamate oxaloacetate transaminase 1-like protein 1, Transaminase A-like protein 1
Detection Method:
ELISA
Assay Type:
Sandwich
Detection Range:
3.9-250pg/mL
Sensitivity:
3pg/mL
Specificity:
Natural and recombinant human Putative aspartate aminotransferase, cytoplasmic 2
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Assay Procedure:

Research Area:
-
- Data
- Citations
- Publication
- Sequence / 3D
- Feedback Wall (0)
Precision
Intra-assay Precision (Precision within an assay):Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.
Intra-Assay CV: ≤3.3%
Inter-assay Precision (Precision between assays):Three samples of known concentration were tested in five separate assays to assess inter-assay precision.
Inter-Assay CV: ≤5.8%
Recovery
Recovery was determined by spiking various levels of Putative aspartate aminotransferase, cytoplasmic 2 into serum and plasma.
Sample Type |
Average(%) |
Recovery Range(%) |
Serum |
97 |
91-103 |
Plasma |
99 |
93-105 |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Putative aspartate aminotransferase, cytoplasmic 2 and their serial dilutions.
The results were demonstrated by the percentage of calculated concentration to the expected.
Sample |
1:2 |
1:4 |
1:8 |
1:16 |
serum(n=5) |
99-109% |
85-98% |
104-114% |
111-123% |
EDTA plasma(n=5) |
98-108% |
104-112% |
95-104% |
86-97% |
heparin plasma(n=5) |
98-108%
|
109-118% |
89-102% |
87-97% |
General Annotation
Sub Unit:
Homodimer.
Function:
N/A
Subcellular Location:
Cytoplasm
Database link
UniGene:
SMR:
STRING:
KEGG:
Pfam:
Uniprot:
This product has not yet been referenced specifically in any publications.
[1].
"Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences."
[2].
"Architecture of the human interactome defines protein communities and disease networks."
[3].
"Biosynthesis of D-aspartate in mammals: the rat and human homologs of mouse aspartate racemase are not responsible for the biosynthesis of D-aspartate."
[4].
"Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degeneration."
[5].
"Targeted ubiquitination and degradation of G-protein-coupled receptor kinase 5 by the DDB1-CUL4 ubiquitin ligase complex."
[6].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."
[8].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
[9].
"Localization of the structural genes for hexokinase-1 and inorganic pyrophosphatase on region (pter-->q24) of human chromosome 10."
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