|
DNA Synthesis and Repair
Proteins Antibodies
ADI has produced highly specific rabbit
polyclonal and mouse monoclonal antibodies to various proteins involved
in DNA Synthesis and repair.
|
Items |
Antigen/
peptide
location |
Ab
Host |
*Expected Ab
Crossreactivity |
Antiserum
Cat #
(100 ul) |
Aff. Pure /Mono
Cat # (100 ug) |
* Control Peptide
Cat#
(100 ug) |
|
Ape ab #1 |
h, Apex protein |
Rb, poly |
h (m, r?) |
APE11-S |
. |
. |
|
APE pure protein |
Human Recombinant
pure APE protein for WB (inactive),
Cat # APE11-C (100 ul)
Human Recombinant pure APE protein (Active),
Cat # APE25R-5 (5 ug); 10 ug |
|
APE ab # 2 |
M, APE protein |
Rb, poly |
m, r (h?) |
APE12-S |
. |
. |
|
hOGG1 ab # 2 |
h, OGG1 protein |
Rb, poly |
h ,m, r |
HOGG12-S |
. |
. |
|
mOGG1 ab # 3 |
m, 18 aa, NT |
Rb, poly |
m, r |
MOGG13-S |
MOGG13-A
|
MOGG13-P |
|
mOGG1 pure
protein |
Mouse Recombinant
pure mOGG1 protein for WB (inactive),
Cat # MOGG13-C (100 ul)
Mouse Recombinant pure mOGG1 protein (Active),
Cat # mOGG25R-5 (5 ug); 10 ug |
|
hNTH1 ab # 1 |
H, NTh1 protein |
Rb, poly |
H (m, r?) |
HNTH11-S |
. |
. |
|
MGMT ab # 1 |
H, MGMT protein |
Rb, poly |
H (m, r?) |
MGMT11-S |
MGMT11-A |
MGMT11-P |
|
MGMT ab # 2 |
H, MGMT
protein |
M, mono |
H (m, r?) |
|
MGMT12-M |
. |
|
MGMT pure protein
|
Human Recombinant
pure MGMT protein for WB (inactive),
Cat # MGMT12-C (100 ul)
Human Recombinant pure MGMT protein (Active),
Cat # MGMT15-R-10 (5 ug); 10 ug |
mutY homolog
ab # 1 |
H, mutY, 17 aa,
NT |
Rb, poly |
H (m, r?) |
MUTY11-S |
MUTY11-A |
MUTY11-P |
mutY homolog
ab # 2 |
H, mutY, 19 aa,
CT |
Rb, poly |
H (m, r?) |
MUTY12-S |
MUTY12-A |
MUTY12-P |
dsDNA
ab # 1 |
dsDNA |
M, mono |
all species |
. |
DNA11-M |
|
DNA Ligase
ab # 1 |
b, DNA Lig.
Protein |
M, mono |
H, b (m, r?) |
|
DNAL11-M |
|
DNA Pol. beta
ab # 1 |
r, DNA Pol. b
Protein |
M, mono |
r, m, h |
|
DNPB11-M |
|
|
DNA Pol. epsilon
ab # 1 |
h, DNA Pol. e
1-176 aa |
M, mono |
r, m, h |
|
DNPE12-M |
|
|
DNA Pol. gamma ab
# 1 |
h, DNA Pol.
g26-276 aa |
M, mono |
r, m, h |
|
DNPG13-M |
|
DNA Pol
delta ab # 1 |
h 21-aa ~NT |
Rb, poly |
r, m, h, b |
DNPD11-S |
|
DNPS11-P |
DNA Primase
ab # 1 |
m, p49 subunit |
Rb, poly |
m, h |
. |
DNPR13-A |
|
DNA Primase
ab # 1 |
m, p58 subunit |
M, mono |
m, h |
. |
DNPR14-A |
|
DNA Pkcs
ab # 1 |
h, DNA PK |
M, mono |
h |
|
DNPK11-M |
|
|
DNAse I |
bovine, DNAse I |
G, poly |
bovine (m, r, h?) |
. |
DNASE11-A |
DNASE11-C
(100 ul) |
DNAse II
ab # 1 |
h 21-aa ~CT |
Rb, poly |
h |
DNASE21-S |
DNASE21-A |
DNASE21-P |
DNAse II
ab # 2 |
m 17-aa ~CT |
Rb, poly |
m |
DNASE22-S |
DNASE22-A |
DNASE22-P |
Ku70
ab # 1 |
h, Ku 506-541 aa |
M, mono |
h |
|
Ku701-M |
|
Ku80
ab # 1 |
h, Ku 1-374 |
M, mono |
h |
|
Ku801-M |
|
ERCC1
ab # 1 |
h, ERCC1 |
M, mono |
h (m, r?) |
|
ERCC11-M |
|
ORC1
ab # 1 |
h, ORC1 |
M, mono |
h (m, r?) |
|
ORC11-M |
|
XPA
ab # 1 |
h, XPA |
M, mono |
h (m, r?) |
|
XPA11-M |
|
XPG/ERCC5
ab # 1 |
h, XPG |
M, mono |
h (m, r?) |
|
XPG11-M |
|
|
XRCC1 ab # 1 |
h, XRCC1 protein |
M, mono |
h (m, r?) |
|
XRCC11-M |
|
|
Thymine Glycols ab
# 1 |
Mrl autoimmune
mice |
M, mono |
h, m, r |
|
THG11-M |
|
|
Topoisomerase II
a, ab # 1 |
H, 1513-1530 aa |
M, mono |
h, m, r |
|
TOP11-M |
|
|
Thymidylate
Synthase, ab # 1 |
H, TS protein |
M, mono |
H (m, r?) |
|
TS11-M |
|
Thymidine
Phosphoryl,
ab # 1 |
H, TP protein |
M, mono |
M, |
|
THP11-M |
|
|
Control (non-immune) IgGs for
ELISA/Western/IHC etc |
Control Rabbit IgG, Cat #20009; 1
mg
Control Goat IgG, Cat #20011; 1 mg
Control Mouse IgG, Cat #20008; 1 mg |
m=mouse; r=rat; h=human; b=bovine; d=dog; ~CT
or ~NT=near C or N-terminus.
EC=Extracellular;
CP=Cytoplasmic domain;
* Expected antibody crossreactivity
information is mostly based upon high (>70%) sequence
conservation of antigenic/control peptides in various species. When
antibody crossreactivity has actually been experimentally confirmed in
various species, it will be mentioned in the appropriate data sheets.
"Neat Antisera or antisera"
are the unpurified antiserum and it is suitable for ELISA and Western.
"Affinity pure" IgG may be
more suitable for immunohistochemical (IHC) applications and to reduce
background in most immunological applications including ELISA and
Western.
"Control peptides" can not be
used for Western as they are very short peptides. They are intended for
ELISA or antibody blocking studies to establish antibody specificity.
Western blot +ve protein controls,
where available, are semi-pure, pure or recombinant proteins that are
formulated in SDS-PAGE sample buffer (reduced). They are recommended to
be used for Western (load 10 ul/lane) for visulization with antibodies.
All Products are for in vitro
research use only. rev 40415A
List of
publications using ADI's Antibodies to various products involved in DNA
Repair
MGMT Biswas T
1999 Activation of human
O6-methylguanine-DNA methyltransferase gene by glucocorticoid hormone
Oncogene18, 525 - 532 WB, MGMT protein antibodies.
hMYH
Boldogh, Istvan 2001
hMYH cell cycle-dependent expression, subcellular localization and
association with replication foci: evidence suggesting
replication-coupled repair of adenine:8-oxoguanine mispairs Nucleic
Acids Research, 2001, Vol. 29, No. 13 2802-2809 WB other mutY from Dr
Mitra, PCNA from SC.
hNTH1
Liu X and R Roy 2002
Truncation of Amino-terminal Tail Stimulates Activity of Human
Endonuclease III (hNTH1) J. Mol. Biol. 321, 265-276 WB custom antibodies
to proteins.
MYH
# 2 ab Yamane A 2003
Suppressive activities of OGG1 and MYH proteins against G:C to T:A
mutations caused by 8-hydroxyguanine but not by
benzo[[!LB]]a[[!RB]]pyrene diol epoxide in human cells in vivo,
Carcinogenesis, Apr 2003; 561. WB,, ~38 kda and others, ape-1 form
novus.
MYH
# 2 ab Yamaguchi S 2002
A single nucleotide polymorphism at the splice donor site of the human
MYH base excision repair gene results in reduced translation efficiency
of its transcripts Genes to Cells 7 Issue 5 Page 461 WB,, ~38 kda and
others , ape-1 form novus.
hOGG1
Cardozo-Pelaez F eat al 2002
Effects of diethylmaleate on DNA damage and repair in the mouse brain
Free Radical Biology and Medicine 33, 292-298 WB,, ~38 kda and others
mouse brain.
hOGG1
Stedeford, Todd 2001
Comparison of base-excision repair capacity in
proliferating and differentiated PC 12 cells following acute challenge
with dieldrin Free Radical Biol Med 31, 1272-1278 WB, pC12 cells.
hOGG1
Cappelli E et al 2001
Rates of base excision repair are not solely dependent on levels of
initiating enzymes Carcinogenesis 2001 22: 387-393 WB,, ~38 kda and
others, ape-1 form novus.
hOGG1
Hyun J-W 2000
Leukemic cell line, KG-1 has a functional loss of hOGG1 enzyme due to a
point mutation and 8-hydroxydeoxyguanosine can kill KG-1 Oncogene19,
4476 - 4479 WB,, ~38 kda and others.
|