PIPA5113391

SLC52A3 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5113391-Each-of-1 In Stock ₹ 42,853.50

PIPA5113391 - Each of 1

₹ 42,853.50

In Stock

Quantity

1

Base Price: ₹ 42,853.50

GST (18%): ₹ 7,713.63

Total Price: ₹ 50,567.13

Antigen

SLC52A3

Classification

Polyclonal

Conjugate

Unconjugated

Gene

SLC52A3

Gene Alias

2310046K01Rik; bA371L19.1; BVVLS; BVVLS1; C20orf54; ct054; hRFT2; Rft2; RFVT3; RGD1304644; Riboflavin transporter 2; rRFT2; Slc52a3; solute carrier family 52 (riboflavin transporter), member 3; solute carrier family 52 member 3; solute carrier family 52, riboflavin transporter, member 3; solute carrier protein family 52, member 3

Host Species

Rabbit

Purification Method

Protein G

Regulatory Status

RUO

Gene ID (Entrez)

113278, 69698

Content And Storage

-20°C or -80°C if preferred

Form

Liquid

Applications

ELISA, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

3.5 mg/mL

Formulation

PBS with 50% glycerol and 0.03% ProClin 300; pH 7.4

Gene Accession No.

Q9D6X5, Q9NQ40

Gene Symbols

SLC52A3

Immunogen

Recombinant Human Solute carrier family 52, riboflavin transporter, member 3 protein (159-220AA)

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

FEPA5144190

--

Img

Thermo Scientific

PIPA5116867

--

Img

Thermo Scientific

PIPA5104351

--

Img

Thermo Scientific

PA550761

--

Img

Thermo Scientific

PA550789

--

Img

Novus Biologicals

NB320574

--

Img

Thermo Scientific

PA550995

--

Img

Thermo Scientific

PIPA5113782

--

Description

  • This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin
  • The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus
  • Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease
  • [provided by RefSeq, Mar 2012].