PIPA528973

GRHL2 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA528973-Each-of-1 In Stock ₹ 49,439.50

PIPA528973 - Each of 1

₹ 49,439.50

In Stock

Quantity

1

Base Price: ₹ 49,439.50

GST (18%): ₹ 8,899.11

Total Price: ₹ 58,338.61

Antigen

GRHL2

Classification

Polyclonal

Conjugate

Unconjugated

Gene

GRHL2

Gene Alias

0610015A08Rik; BOM; Brother of mammalian grainyhead; DFNA28; ECTDS; grainyhead like 2; grainyhead like transcription factor 2; grainyheadlike; grainyhead-like 2; grainyhead-like 2 (Drosophila); grainyhead-like protein 2 homolog; grainyhead-like transcription factor 2; Grhl2; RGD1561191; Tcfcp2l3; TFCP2L3; transcription factor CP2-like 3

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

79977

Content And Storage

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

Form

Liquid

Applications

Western Blot

Concentration

0.94 mg/mL

Formulation

PBS with 1% BSA, 20% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

Q6ISB3

Gene Symbols

GRHL2

Immunogen

Recombinant fragment corresponding to a region within amino acids 14 and 252 of Human GRHL2

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PIPA529479

--

Img

Thermo Scientific

PIPA529137

--

Img

Thermo Scientific

PIPA528981

--

Img

Thermo Scientific

PIPA530165

--

Img

Thermo Scientific

PIPA528860

--

Img

Thermo Scientific

PIPA529394

--

Img

Thermo Scientific

PIPA529529

--

Img

Thermo Scientific

PIPA529072

--

Description

  • Recommended positive controls: NT2D1, U87-MG
  • Predicted reactivity: Mouse (90%), Rat (90%)
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3
  • Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).