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PIPA584361

MED26 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA584361-Each-of-1 In Stock ₹ 52,332.00

PIPA584361 - Each of 1

₹ 52,332.00

In Stock

Quantity

1

Base Price: ₹ 52,332.00

GST (18%): ₹ 9,419.76

Total Price: ₹ 61,751.76

Antigen

MED26

Classification

Polyclonal

Conjugate

Unconjugated

Gene

MED26

Gene Alias

5730493L18Rik, Activator-recruited cofactor 70 kDa component, AI414941, ARC70, AW495270, cofactor required for Sp1 transcriptional activation subunit 7, cofactor required for Sp1 transcriptional activation, subunit 7 (70kD), cofactor required for Sp1 transcriptional activation, subunit 7, 70kDa, CRSP complex subunit 7, Crsp7, CRSP70, Med26, Mediator complex subunit 26, mediator of RNA polymerase II transcription subunit 26, Slc35e1, solute carrier family 35, member E1, transcriptional coactivator CRSP70

Host Species

Rabbit

Purification Method

Anitgen affinity chromatography, Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

9441

Content And Storage

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

Form

Liquid

Applications

Immunohistochemistry

Concentration

0.2 mg/mL

Formulation

PBS with 40% glycerol and 0.02% sodium azide, pH 7.2

Gene Accession No.

O95402

Gene Symbols

MED26

Immunogen

Recombinant protein corresponding to Human MED26

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Description

  • Immunogen sequence: PGAHHFMSEY LKQEESTRQG ARQLHVLVPQ SPPTDLPGLT REVTQDDLDR IQASQWPGVN GCQDTQGNWY DWT This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B signaling pathway
  • The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals
  • Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene
  • Mutations in this gene result in sporadic and familial Paget disease of bone.