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Base excision repair

pathways : Base excision repair pathways:

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Related Pathways to "Base excision repair" content :


Related Genes to "Base excision repair" content :

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Catalog number Product name Quantity
26-948 POLL is a repair polymerase.It is involved in base excision repair (BER) responsible for repair of lesions that give rise to abasic (AP) sites in DNA. Has both DNA polymerase and terminal transferase 0.05 mg
26-841 Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutation 0.05 mg
3863 (CT) a major enzyme in the base excision repair pathway 0.5 mg
3865 (NT) a major enzyme in the base excision repair pathway 0.5 mg
3861 (IN) a major enzyme in the base excision repair pathway 0.5 mg
3865 (NT) a major enzyme in the base excision repair pathway 0.1 mg
3859 (NT) a major enzyme in the base excision repair pathway 0.5 mg
3863 (CT) a major enzyme in the base excision repair pathway 0.1 mg
3861 (IN) a major enzyme in the base excision repair pathway 0.1 mg
3859 (NT) a major enzyme in the base excision repair pathway 0.1 mg
EREG ERCM1 Gene excision repair complementing defective repair in mouse cells
EIAAB46543 DNA excision repair protein ERCC-4,DNA repair endonuclease XPF,Ercc4,Mouse,Mus musculus
GS-0704a excision repair cross-complementing rodent repair primary antibody, Host: Rabbit 200ul
GS-0705a excision repair cross-complementing rodent repair primary antibody, Host: Rabbit 200ul
E-EL-H1853 Human ERCC1 (Excision Repair Cross Complementing Rodent Repair Deficiency Complementation 1) ELISA Kit 96T
ERCM1 ERCC6L Gene excision repair cross-complementing rodent repair deficiency, complementation group 6-like
ERCC6L ERCC5 Gene excision repair cross-complementing rodent repair deficiency, complementation group 5
ERCC6 ERCC4 Gene excision repair cross-complementing rodent repair deficiency, complementation group 4
E-EL-P1011 Porcine ERCC1 (Excision Repair Cross Complementing Rodent Repair Deficiency Complementation 1) ELISA Kit 96T
ERCC4 ERCC2 Gene excision repair cross-complementing rodent repair deficiency, complementation group 2
ERDA1 ERCC8 Gene excision repair cross-complementing rodent repair deficiency, complementation group 8
E-EL-Ch1395 Chicken ERCC1 (Excision Repair Cross Complementing Rodent Repair Deficiency Complementation 1) ELISA Kit 96T
ERCC8 ERCC6 Gene excision repair cross-complementing rodent repair deficiency, complementation group 6
26-847 LIG1is DNA ligase I, with functions in DNA replication and the base excision repair process. Mutations in LIG1 that lead to DNA ligase I deficiency result in immunodeficiency and increased sensitivity 0.05 mg
SEG627Hu ELISA Kit for Excision Repair Cross Complementing Rodent Repair Deficiency Complementation 1 (ERCC1) Homo sapiens (Human) 96T

Pathways :

WP1625: Base excision repair
WP1787: Base Excision Repair
WP1678: Nucleotide excision repair
WP1980: Nucleotide Excision Repair
WP1035: Mismatch repair
WP1152: Mismatch repair
WP1204: Mismatch repair
WP1215: Mismatch repair
WP1233: Mismatch repair
WP1257: Mismatch repair
WP1295: Mismatch repair
WP1361: Mismatch repair
WP1672: Mismatch repair
WP1805: DNA Repair
WP1807: Double-Strand Break Repair
WP531: Mismatch repair
WP740: Mismatch repair
WP802: Mismatch repair
WP916: Mismatch repair

Related Genes :
[ERCC2 XPD XPDC] General transcription and DNA repair factor IIH helicase subunit XPD (TFIIH subunit XPD) (EC 3.6.4.12) (Basic transcription factor 2 80 kDa subunit) (BTF2 p80) (CXPD) (DNA excision repair protein ERCC-2) (DNA repair protein complementing XP-D cells) (TFIIH basal transcription factor complex 80 kDa subunit) (TFIIH 80 kDa subunit) (TFIIH p80) (Xeroderma pigmentosum group D-complementing protein)
[ERCC4 ERCC11 XPF] DNA repair endonuclease XPF (EC 3.1.-.-) (DNA excision repair protein ERCC-4) (DNA repair protein complementing XP-F cells) (Xeroderma pigmentosum group F-complementing protein)
[ERCC3 XPB XPBC] General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (Basic transcription factor 2 89 kDa subunit) (BTF2 p89) (DNA excision repair protein ERCC-3) (DNA repair protein complementing XP-B cells) (TFIIH basal transcription factor complex 89 kDa subunit) (TFIIH 89 kDa subunit) (TFIIH p89) (Xeroderma pigmentosum group B-complementing protein)
[Ercc1 Ercc1_predicted rCG_54407] ERCC excision repair 1, endonuclease non-catalytic subunit (Excision repair cross-complementing rodent repair deficiency, complementation group 1 (Predicted), isoform CRA_a)
[Ercc3 Xpb Xpbc] General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (Basic transcription factor 2 89 kDa subunit) (BTF2 p89) (DNA excision repair protein ERCC-3) (DNA repair protein complementing XP-B cells) (TFIIH 89 kDa subunit) (Xeroderma pigmentosum group B-complementing protein)
[Ercc2 Xpd] General transcription and DNA repair factor IIH helicase subunit XPD (TFIIH subunit XPD) (EC 3.6.4.12) (CXPD) (DNA excision repair protein ERCC-2) (DNA repair protein complementing XP-D cells) (Xeroderma pigmentosum group D-complementing protein)
[ERCC6 CSB] DNA excision repair protein ERCC-6 (EC 3.6.4.-) (ATP-dependent helicase ERCC6) (Cockayne syndrome protein CSB)
[ERCC5 ERCM2 XPG XPGC] DNA repair protein complementing XP-G cells (EC 3.1.-.-) (DNA excision repair protein ERCC-5) (Xeroderma pigmentosum group G-complementing protein)
[ERCC2 XPD] General transcription and DNA repair factor IIH helicase subunit XPD (TFIIH subunit XPD) (EC 3.6.4.12) (CXPD) (DNA excision repair protein ERCC-2) (DNA repair protein complementing XP-D cells) (Xeroderma pigmentosum group D-complementing protein)
[RAD23B] UV excision repair protein RAD23 homolog B (HR23B) (hHR23B) (XP-C repair-complementing complex 58 kDa protein) (p58)
[ERCC2] General transcription and DNA repair factor IIH helicase subunit XPD (TFIIH subunit XPD) (EC 3.6.4.12) (CXPD) (DNA excision repair protein ERCC-2) (DNA repair protein complementing XP-D cells) (Xeroderma pigmentosum group D-complementing protein)
[Ercc4] DNA repair endonuclease XPF (EC 3.1.-.-) (DNA excision repair protein ERCC-4)
[ERCC3] General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (DNA excision repair protein ERCC-3)
[Ercc5 Ercc-5 Xpg] DNA repair protein complementing XP-G cells homolog (EC 3.1.-.-) (DNA excision repair protein ERCC-5) (Xeroderma pigmentosum group G-complementing protein homolog)
[hay ERCC3 CG8019] General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (ATP-dependent DNA helicase hay) (DNA excision repair protein haywire) (ERCC-3 homolog protein) (ERCC3Dm)
[Ercc3] General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (DNA excision repair protein ERCC-3)
[Rad23b Mhr23b] UV excision repair protein RAD23 homolog B (HR23B) (mHR23B) (XP-C repair-complementing complex 58 kDa protein) (p58)
[repD ercc2 DDB_G0267414] General transcription and DNA repair factor IIH helicase subunit XPD (TFIIH subunit XPD) (EC 3.6.4.12) (DNA excision repair cross-complementing protein-2 homolog) (DNA repair protein D) (TFIIH basal transcription factor complex helicase repD subunit)
[UVH1 RAD1 At5g41150 MEE6.22] DNA repair endonuclease UVH1 (EC 3.1.-.-) (DNA excision repair protein XP-F homolog) (Ultraviolet hypersensitive 1) (AtRAD1)
[ERCC1] DNA excision repair protein ERCC-1
[Ercc6] Excision repair cross-complementing rodent repair deficiency, complementation group 6 (Fragment)
[Ercc6] Excision repair cross-complementing rodent repair deficiency, complementation group 6
[Ercc1 Ercc-1] DNA excision repair protein ERCC-1
[ERCC1] DNA excision repair protein ERCC-1
[ERCC8 CKN1 CSA] DNA excision repair protein ERCC-8 (Cockayne syndrome WD repeat protein CSA)
[ERCC4] DNA repair endonuclease XPF (EC 3.1.-.-) (DNA excision repair protein ERCC-4)
[repB ercc3 DDB_G0278729] General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (DNA excision repair cross-complementing protein-3 homolog) (DNA repair helicase repB) (DNA repair protein B)
[RAD23A] UV excision repair protein RAD23 homolog A (HR23A) (hHR23A)
[RAD23 YEL037C SYGP-ORF29] UV excision repair protein RAD23
[Rad23a Mhr23a] UV excision repair protein RAD23 homolog A (HR23A) (mHR23A)

Bibliography :
[30999232] A method for the cell-cycle-specific analysis of radiation-induced chromosome aberrations and breaks.
[30999038] Reconciling the controversial data on the effects of C fullerene at the organismal and molecular levels using as a model Drosophila melanogaster.
[30998989] Methylation Tolerance-based Functional Assay to Assess Variants of Unknown Significance in the MLH1 and MSH2 Genes and Identify Patients With Lynch Syndrome.
[30998688] Ribosomal RNA gene repeats associate with the nuclear pore complex for maintenance after DNA damage.
[30998678] MAW point mutation impairs H. Seropedicae RecA ATP hydrolysis and DNA repair without inducing large conformational changes in its structure.
[30998513] Poly (ADP-ribose) polymerase inhibitors combined with other small-molecular compounds for the treatment of ovarian cancer.
[30998386] Deficiency of X-ray repair cross-complementing group 1 in primordial germ cells contributes to male infertility.
[30998359] Novel deazaflavin analogues potently inhibited tyrosyl DNA phosphodiesterase 2 (TDP2) and strongly sensitized cancer cells toward treatment with topoisomerase II (TOP2) poison etoposide.
[30997620] Proteasome inhibitors trigger mutations via activation of caspases and CAD, but mutagenesis provoked by the HDAC inhibitors vorinostat and romidepsin is caspase/CAD-independent.
[30997540] Influence of XRCC4 expression by breast cancer cells on ipsilateral recurrence after breast-conserving therapy.