Invitrogen

XPD Polyclonal Antibody

View all (19) XPD antibodies

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Datasheet
Protocols
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Datasheet
Protocols
Questions & Answers

Product Details

PA5-120282

Applications
Tested Dilution
Publications

Western Blot (WB)

1:500-1:1,000
-

ELISA (ELISA)

1 µg/mL
-
Product Specifications

Species Reactivity

Human, Mouse, Rat

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human XPD/XPD/ERCC2 (NP_0011243391)
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Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

0.69 mg/mL

Purification

Affinity Chromatography

Storage buffer

PBS, pH 7.3, with 50% glycerol

Contains

0.05% ProClin 300

Storage conditions

-20°C, Avoid Freeze/Thaw Cycles

Shipping conditions

Wet ice

RRID

AB_2913854

Product Specific Information

Positive test controls include: HeLa, K-562, 293T, MCF7, mouse lung, mouse testis, rat testis. The target is usually found in the following locations: Cytoplasm, Nucleus, cytoskeleton, spindle.

Immunogen sequence: MRELKRTLDA KGHGVLEMPS GTGKTVSLLA LIMAYQRAYP LEVTKLIYCS RTVPEIEKVI EELRKLLNFY EKQEGEKLPF LGLALSSRKN LCIHPEVTPL RFGKDVDGKC HSLTASYVRA QYQHDTSLPH CRFYEEFDAH GREVPLPAGI YNLDDLKALG RRQGWCPYFL ARYSILHANV

Target Information

XPD is involved with the nucleotide excision repair pathway that is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: Basic transcription factor 2 80 kDa subunit; BTF2 p80; CXPD; DNA 5'-3' helicase XPD; DNA excision repair protein ERCC-2; DNA repair protein complementing XP-D cells; excision repair cross-complementation group 2; excision repair cross-complementing rodent repair deficiency, complementation group 2; General transcription and DNA repair factor IIH helicase subunit XPD; MGC102762; MGC126218; MGC126219; TFIIH 80 kDa subunit; TFIIH basal transcription factor complex 80 kDa subunit; TFIIH basal transcription factor complex helicase subunit; TFIIH basal transcription factor complex helicase XPB subunit; TFIIH basal transcription factor complex helicase XPD subunit; TFIIH p80; TFIIH subunit XPD; xeroderma pigmentosum complementary group D; Xeroderma pigmentosum group D-complementing protein

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Gene Aliases: AA407812; AU020867; AW240756; COFS2; CXPD; EM9; Ercc-2; ERCC2; TFIIH; TTD; TTD1; XPD; XPDC

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UniProt ID: (Human) P18074, (Mouse) O08811

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Entrez Gene ID: (Human) 2068, (Mouse) 13871, (Rat) 308415

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Function(s)
DNA binding ATP-dependent DNA helicase activity protein kinase activity protein binding ATP binding protein C-terminus binding DNA-dependent ATPase activity RNA polymerase II carboxy-terminal domain kinase activity 5'-3' DNA helicase activity metal ion binding protein N-terminus binding 4 iron, 4 sulfur cluster binding nucleotide binding nucleic acid binding helicase activity ATP-dependent helicase activity hydrolase activity hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides iron-sulfur cluster binding molecular_function
Process(es)
in utero embryonic development nucleobase-containing compound metabolic process DNA repair transcription-coupled nucleotide-excision repair nucleotide-excision repair transcription, DNA-templated regulation of transcription, DNA-templated transcription from RNA polymerase II promoter protein phosphorylation apoptotic process cellular response to DNA damage stimulus response to oxidative stress chromosome segregation aging cell proliferation response to UV UV protection post-embryonic development spinal cord development hair cycle process extracellular matrix organization bone mineralization central nervous system myelin formation DNA duplex unwinding nucleotide-excision repair, DNA incision multicellular organism growth hair cell differentiation embryonic cleavage erythrocyte maturation positive regulation of DNA binding skin development positive regulation of transcription, DNA-templated positive regulation of transcription from RNA polymerase II promoter hair follicle maturation hematopoietic stem cell differentiation regulation of mitotic cell cycle phase transition nucleotide-excision repair, DNA duplex unwinding response to hypoxia nucleotide-excision repair, preincision complex stabilization nucleotide-excision repair, preincision complex assembly nucleotide-excision repair, DNA incision, 3'-to lesion nucleotide-excision repair, DNA incision, 5'-to lesion transcription initiation from RNA polymerase I promoter transcription elongation from RNA polymerase I promoter termination of RNA polymerase I transcription transcription initiation from RNA polymerase II promoter transcription elongation from RNA polymerase II promoter 7-methylguanosine mRNA capping viral process global genome nucleotide-excision repair
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