PA550936

CLN5 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA550936-Each-of-1 In Stock ₹ 46,057.50

PA550936 - Each of 1

₹ 46,057.50

In Stock

Quantity

1

Base Price: ₹ 46,057.50

GST (18%): ₹ 8,290.35

Total Price: ₹ 54,347.85

Antigen

CLN5

Classification

Polyclonal

Conjugate

Unconjugated

Gene

CLN5

Gene Alias

A730075N08Rik; ceroid-lipofuscinosis; Ceroid-lipofuscinosis neuronal protein 5; ceroid-lipofuscinosis neuronal protein 5 homolog; Ceroid-lipofuscinosis neuronal protein 5 homolog, secreted form; Ceroid-lipofuscinosis neuronal protein 5, secreted form; ceroid-lipofuscinosis, neuronal 5; CLN5; NCL; Protein CLN5

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

1203, 211286, 306128

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

ELISA, Western Blot

Concentration

1 mg/mL

Formulation

PBS with 0.5% BSA, 50% glycerol and 0.02% sodium azide; pH 7.4

Gene Accession No.

O75503, Q3UMW8

Gene Symbols

CLN5

Immunogen

Synthesized peptide derived from the Internal region of human CLN5.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PA551123

--

Img

Thermo Scientific

PA551118

--

Img

Thermo Scientific

PA551050

--

Img

Thermo Scientific

PA551023

--

Img

Thermo Scientific

PA550934

--

Img

Thermo Scientific

PA551048

--

Img

Thermo Scientific

PA551051

--

Img

Thermo Scientific

PA550927

--

Description

  • CLN5 Polyclonal Antibody detects endogenous levels of CLN5 protein
  • This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL)
  • Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children
  • The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes
  • The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008].