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ALT range
0-55 IU/L
AST range
5-34 IU/L
LD range
125-220 IU/L
AlkP range
40-150 IU/L (higher in kids)
GGT range
12-64 IU/L M 9-36 F
Bilirubin total range
0.1-1.2 mg/dL
Bilirubin total critical
>15.0 NEONATES
Bilirubin direct range
0-0.5
Bilirubin indirect range
0-0.6
amylase range
25-125 IU/L Serum 1-17 urine
Lipase range
8-78 IU/L
Uric acid range
2.6-7.2
Ethanol range
0-10 mg/dL
Ammonia range
18-72 umol/L
ALT methodology
L- alanine and alpha ketogluterate to pyruvate L-glutamate, NADH oxidized to NAD and lactate (LD enzyme)
AST methodology
L aspartate and alpha keto to oxaloacetata and L glutamate, oxidize to malate with MDH enzyme
LD methodology
L lactate and NAD to pyruvate and NADH (reversible)
ALP methodology
P-nitrophenylphosphate and water to P-nitrophenol
GGT methodology
gamma glutamyl 3- carboxy-4 nitroalimide and glycylglycine to gamma glycylglycide 3- carboxy- 4 nitroalimide
Bilirubin methodology
react with sodium nitrate to make biliverdin
Ammonia methodolgy
NH and NADH and alpha-k to glutamate and NAD (GLDH enzyme)
Ethanol methodology
____ and NAD with ADH to reduce NADH and acetaldehyde
Amylase methodology
CNPG3 to CPNP and CNOG2 and maltortiose and glucose
Lipase methodology
lipase, MGLP, GPO, HPO (horseradish peroxidase) and ox coupling of
Bili critical
>15 neonate
Na methodology
Crown Ether ionophore ICT tech
K methodology
Valinomycin in ion selective mb ICT tech
Cl methodology
Silver chloride disk establishing equilibrium. calculating Ksp from the conc with excess soluble AgCl then interpreted by ICT
Na range
136-145 meq/L
Na critical
>160 <120
K range
3.5-5.1 mmol/L
K critical
< 3 <6
Cl range
98-107 meq/L
Serum CO2 methodology
Bicaarb and PEP convert to oxalacetate and phosphate by PEPC. Then the oxa and NADH are reduced to Malate and NAD by MDH. (Abs proportional to the _____ in sample.
CO2 range
22-33 meq/L
CO2 critical
<10
Wavelength that NADH and NADPH peak seen
340nm
Anion Gap
Conc of cations and anions must be equal
Anion Gap with K range
10-20 mmol/L
Anion Gap no K
7-16 mmol/L
OSMO
280-300 mOsm/kg
Osmo gap above 10 is indicative of what?
paraproteins or alcohol, when present will contribute to what ____ gap?
BUN
Blood urea nitrogen
BUN methodology
Kinetic assay. Urea hydrolyzed to NH3 and CO2, then rxt with alpha-ketogluterate to reduce to NAD and glutamate. (uses urease and GLD)
BUN ranges
9-21 male. 7-19 female mg/dL
What element inhibits urease
flouride (connection to BUN rxn)
Creatinine methodology
Jaffes rxn (picric acid and ALK for a red color)
Creatinine range
0.7-1.4 mg/dL
Plasma creatinine and GFR relationship
inverse
Glucose methodology
_____ rxts due to hexokinase with ATP and Mg to produce G6P that then reacts due to G6PD to reduce to 6-Phosphogluconate and NADH
Glucose range
70-125mg/dL
Glucose critical
<40 >400
Hgb A1C shows results for what time frame of blood glucose
2-3 months (lifespan of RBC)
A1c range
4-5.6%
A1C methodology
enzymatic (glycated Hgb and total hgb)
Uric Acid range
2.6-7.2 mg/dL
Uric acid methodology
uricase ox. for allantoin and hydrogen peroxide. a peroxidase with AAP results in a quinonimine dye
How is uric acid produced in body
The breakdown of purines…. produce what?
Cholesterol range
<200mg/dL
Cholesterol methodology
_____ esterase hydrolyzes to 4-3. with HBA and 4AAP to form a dye
Triglyceride range
40-200 mg/dL
Triglyceride methodology
lipase enzyme results in fatty acids and glycerol to then further reacts till you get dihydroxyacetone with 4AAP for a red dye (no peroxidase0
HDL methodology
2 reagent format, to release ____ to rxt with esterase and oxidase chol, witht he presence of chromogen to produce a color due to reaction with peroxidase
HDL range
38-75 male 33-98 female
LDL methodology
2- reagent format (R1 and R2) solubilizes and then chromogen allows color formation
LDL range
<150 mg/dL