PIPA5111287

EML1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5111287-Each-of-1 In Stock ₹ 48,905.50

PIPA5111287 - Each of 1

₹ 48,905.50

In Stock

Quantity

1

Base Price: ₹ 48,905.50

GST (18%): ₹ 8,802.99

Total Price: ₹ 57,708.49

Antigen

EML1

Classification

Polyclonal

Formulation

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

Gene Accession No.

O00423

Gene Symbols

EML1

Immunogen

Recombinant Protein corresonding to Human EML1

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Applications

Immunohistochemistry

Conjugate

Unconjugated

Gene

EML1

Gene Alias

1110008N23Rik; A930030P13Rik; AA171013; AI847476; AI853955; echinoderm microtubule associated protein like 1; echinoderm microtubule associated protein-like protein 1; echinoderm microtubule-associated protein-like 1; ELP79; EMAP; EMAP1; EMAP-1; EMAPL; EMAPL1; Eml1; HuEMAP; huEMAP-1

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

2009

Content And Storage

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

Form

Liquid

Related Products

Img

Thermo Scientific

PIPA5111314

--

Img

Thermo Scientific

PIPA5111516

--

Img

Thermo Scientific

PIPA5111420

--

Img

Thermo Scientific

PIPA5111636

--

Img

Thermo Scientific

PIPA5111383

--

Img

Thermo Scientific

PIPA5111345

--

Img

Thermo Scientific

PIPA5111700

--

Img

Thermo Scientific

PIPA5111686

--

Description

  • Immunogen sequence: SGVRKETAVP ATKSNIKRTS SSERVSPGGR RESNGDSRGN RNRTGSTSSS Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene
  • Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type
  • The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems
  • The USHs are categorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3)
  • The type I is the most severe form
  • Gene loci responsible for these three types are all mapped
  • Two transcript variants encoding different isoforms have been found for this gene.