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79 Cards in this Set

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Has receptors for h. pylori

leb

marker for reed sternberg cell of hodgkin dse

lex

two loci system

MNSs U

ISBT for MNSsU

MN:002

glycophlorin A

MN

glycophorin B

Ss

present when Ss is expressed

U

leucine and glutamic acid on pos 1&5

N ag

M ag amino asid residue

serine and glycine

amino acid residue of S

Methionine

amino acid residue of s

Threonine

Seen on renal px undergoing dialysis with equips sterilized with formaldehyde

Anti N

pH where anti M is active

6.0 to 6.5

what CHO chain is P, P1, and pK related to

ABH and I

chromosome number where P ag is located

chromosome 22

which of the three p ag is poorly developed at birth

P1

P1 can be neutralized by

soluble p1 subs found on hydatid cyst

Antibody of what blood ag has biphasic property

Anti-P

antibody assoc with spontaneous abortion

Anti-PP1 pK

ISBT of I blood group system

I:027

Chromosome number where I is found

chromosome 6

Assoc with much greater i activity on red cells than control cord cells

CDA type II or HEMPAS

May develop strong cold ab with auto anti I specificity

M. pneumoniae

Assoc with Infectious mononucleosis

Anti-i

ISBT of kell system

KEL:006

chromosome number of kell system

chromosome number 7

Second to D antigen in immunogenecity

K antigen

What are the three sulfhydryl reagents that can destroy kell antigen

ZZAP, DTT, AET

meaning of AET

2-aminoethylthiolisothiouroniumbromide

most common antibody seen in bb

Anti-K

lacks Kx antigen

McLeod phenotype

disease assoc with lack of Kx antigen in wbc

CGD

disease assoc with lack of Kx ag in RBC

McLeod syndrime

McLeod syndrome is assoc with

Chronic but well compensated hemolytic anemia


Reticulocytosis & acanthocytosis


CGD


Muscular dystrophy

Kx ag in K null

Abundant

Kx ag in McLeod

Minimal/lacking

Autosomal kell ag in k null

lacking

autosomal kell antigen in McLeod

decreased expression

give 5 other kell ag with assigned letter for each

Cellano (k)


Penny (Kpa)


Rautenberg(Kpb)


Sutter(Jsa)


Class(KL)

ISBT of duffy

FY:008

Chromosome number where duffy ag is located

chromosome 1

most important​ anthropological marker for african blacks

Fy (a-b-)

Where does Fy (a-b-) resistant to

P. vivax and P. knowlesi

ISBT of kidd

JK:009

found on chromosome 18

Jka and Jkb

serves as cell membrane channel for entry of urea to the cell

Jka and Jkb

resists lysis in 2M urea and common in mongoloids

Jk (a-b-)

common cause of delayed HTR

Kidd antobodies

most notorious antibody in bb

Kidd antibodies

phenomenon where ab reacts strongly with red cell carrying double dose than red cell carrying single dose

Dosage effect

ISBT of lutheran

LU:005

chromosome number where lutheran is located

19

3 genetic backgrounds assoc with Lu (a-b-)

Dominant In(Lu)


Recessuve Lulu type


Recessive sex linked inhibitor type

commonly IgG3 antibodies

Kidd antibodies

commonly IgG4 antibodies

Anti-Lub

ISBT of diego system

DI:010

tool used in determining mongolian ancestry

Dia antigen

found in Anion exchange molecule

Dia &Dib

Antigenic determinants of human complement C4

CH/RG antigen

ISBT of Xg system

XG:012

prevalent in women and assoc with multiple transfusion

Xga allele

System with no assoc ISBT

Bg system

Related to HLA antigen

Bg system

Bga

HLA-B7

Bgb

HLA-B17

Bgc

HLA-A28

Anti-Bg is destroyed by

chloroquine diphosphate or glycine-HCl/EDTA soln

ASSOC with DAF

CROMER

Assoc with ADP-ribosyltransferase 4

DOMBROCK

produced in glycophorin C and D

Gerbich

GE:070

Assoc with CD 44

Indian

IN:023

assoc with erythroblast membrane assoc protein

Scianna

SC:013

found on protein acetylcholinesterase

Cartwright

YT:055

Biochemically resembles uromodulin

Sd antigen

Igm abs that can become IgG

LePILuP1

IgG immune abs

KFyJkSsXga

Blood groups assoc with secretor gene

LeLuABH

enhanced by proteolytic enzyme

Kidd


Rh


I


P1


Lewis

Destroyed by proteolytic enzyme

Duffy


MNSs U