PA550876

SERPINB11 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA550876-Each-of-1 In Stock ₹ 46,502.50

PA550876 - 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

SERPINB11

Classification

Polyclonal

Conjugate

Unconjugated

Gene

SERPINB11

Gene Alias

2310046M08Rik; AU015399; EPIPIN; serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 11; serine (or cysteine) proteinase inhibitor, clade B (ovalbumin), member 11; serpin B11; serpin family B member 11 (gene/pseudogene); serpin peptidase inhibitor, clade B (ovalbumin), member 11; SERPIN11; SERPINB11

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

66957, 89778

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1.2 mg/mL

Formulation

PBS with 40% glycerol and 0.05% sodium azide; pH 7.4

Gene Accession No.

Q96P15, Q9CQV3

Gene Symbols

SERPINB11

Immunogen

Fusion protein of human serpin peptidase inhibitor, clade B (ovalbumin), member 11 (gene/pseudogene)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • The antibody detects endogenous levels of total SERPINB11 protein
  • SerpinB11 (serpin peptidase inhibitor, clade B (ovalbumin), member 11), also known as EPIPIN or SERPIN11, is a 392 amino acid cytoplasmic protein that belongs to the Ov-serpin subfamily and serpin family
  • Like other members of the serpin family, SerpinB11 has been identified as a noninhibitory intracellular protein
  • The gene encoding SerpinB11 maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases
  • There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.