PIMA531521

TDG Monoclonal Antibody (GT311), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA531521-Each-of-1 In Stock ₹ 47,481.50

PIMA531521 - Each of 1

₹ 47,481.50

In Stock

Quantity

1

Base Price: ₹ 47,481.50

GST (18%): ₹ 8,546.67

Total Price: ₹ 56,028.17

Antigen

TDG

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with no preservative

Gene Accession No.

P56581, Q13569

Gene Symbols

TDG

Immunogen

Recombinant protein encompassing a sequence within the center region of human TDG.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG2a

Applications

Immunohistochemistry (Paraffin), Western Blot

Clone

GT311

Conjugate

Unconjugated

Gene

TDG

Gene Alias

C-JUN leucine zipper interactive protein JZA-3; E130317C12Rik; G/T mismatch-specific thymine DNA glycosylase; hTDG; Jza1; JZA-3; Tdg; thymine DNA glycosylase; thymine-DNA glycosylase

Host Species

Mouse

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

21665, 6996

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

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Description

  • Keep as concentrated solution
  • Predicted reactivity: Mouse (100%), Rat (99%), Xenopus laevis (92%), Chicken (95%), Bovine (99%)
  • Positive Control: human TDG -transfected 293T
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • The protein encoded by this gene belongs to the TDG/mug DNA glycosylase family
  • Thymine-DNA glycosylase removes thymine moieties from G/T mismatches by hydrolyzing the carbon-nitrogen bond between the sugar-phosphate backbone of DNA and the mis paired thymine
  • With lower activity, this enzyme also removes thymine from C/T and T/T mispairings
  • TDG can also remove uracil and 5-bromouracil from mispairings with guanine
  • This enzyme plays a central role in cellular defense against genetic mutation caused by the spontaneous deamination of 5-methylcytosine and cytosine
  • This gene may have a pseudogene in the p arm of chromosome 12.