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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.
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
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