PA146474

TRPML1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA146474-Each-of-1 In Stock ₹ 46,947.50

PA146474 - Each of 1

₹ 46,947.50

In Stock

Quantity

1

Base Price: ₹ 46,947.50

GST (18%): ₹ 8,450.55

Total Price: ₹ 55,398.05

Antigen

TRPML1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

MCOLN1

Gene Alias

2210015I05Rik; MCLN1; Mcoln1; MCOLN1 mucolipin 1; MG-2; MGC7172; ML1; ML4; MLIV; MST080; MSTP080; Mucolipidin; mucolipidosis type IV protein; mucolipin 1; mucolipin-1; Transient receptor potential channel mucolipin 1; Transient receptor potential-mucolipin 1; TRPML1; TRP-ML1; TRPM-L1

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

288371, 57192, 94178

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

1.0 mg/mL

Formulation

PBS with 0.02% sodium azide

Gene Accession No.

Q99J21, Q9GZU1

Gene Symbols

MCOLN1

Immunogen

Synthetic peptide corresponding to residues 500-580 of a C-terminal portion of mouse Mucolipin-1. [Swiss-Prot# Q99J21]

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PA146294

--

Img

Thermo Scientific

PA146216

--

Img

Thermo Scientific

PA540109

--

Img

Thermo Scientific

PA540133

--

Img

Thermo Scientific

PA146217

--

Img

Thermo Scientific

PA146018

--

Img

Thermo Scientific

PA540127

--

Img

Thermo Scientific

PA146017

--

Description

  • The target sequence has 85% sequence homology with monkey and 78% sequence homology with bovine
  • Suggested positive control: mouse brain protein
  • Defects in Mucolipin-1 are the cause of mucolipidosis type IV (MLIV), also known as sialolipidosis
  • MLIV is an autosomal recessive lysosomal storage disorder characterized by severe psychomotor retardation and ophthalmologic abnormalities, including corneal opacity, retinal degeneration and strabismus
  • Storage bodies of lipids and water-soluble substances are seen by electron microscopy in almost every cell type of the patients
  • Most patients are unable to speak or walk independently and reach a maximal developmental level of 1-2 years
  • All patients have constitutive achlorhydia associated with a secondary elevation of serum gastrin levels.