PIPA5103593

SERPINA2 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5103593-Each-of-1 In Stock ₹ 46,502.50

PIPA5103593 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

SERPINA2

Classification

Polyclonal

Conjugate

Unconjugated

Gene

SERPINA2

Gene Alias

ARGS; ATR; PIL; psiATR; putative alpha-1-antitrypsin-related protein; serine (or cysteine) proteinase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 2; serpin A2; serpin family A member 2 (gene/pseudogene); serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 2, pseudogene; SERPINA2; SERPINA2P

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

390502

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

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

Gene Accession No.

P20848

Gene Symbols

SERPINA2

Immunogen

A synthesized peptide derived from human SERPINA2(Accession P20848), corresponding to amino acid residues K151-H201.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PIPA5102769

--

Img

Thermo Scientific

PIPA5102428

--

Img

Thermo Scientific

PIPA5102996

--

Img

Thermo Scientific

PIPA5102788

--

Img

Thermo Scientific

PIPA5103440

--

Img

Thermo Scientific

PIPA5103132

--

Img

Thermo Scientific

PIPA5102806

--

Img

Thermo Scientific

PIPA5102420

--

Description

  • Antibody detects endogenous levels of total SERPINA2
  • The SERPINA2 gene encodes a member of the serpin family of proteins, a group of proteins that inhibit serine proteases
  • The encoded intracellular glycoprotein is localized at the endoplasmic reticulum
  • This gene is a polymorphic pseudogene, with the non-functional allele being predominant in some populations
  • Some individuals, as represented by the reference genome allele, contain a 2kb coding region deletion and a start code mutation
  • [provided by RefSeq, Feb 2014].