PIMA526752

CANT1 Monoclonal Antibody (OTI7F8), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA526752-Each-of-1 In Stock ₹ 52,198.50

PIMA526752 - Each of 1

₹ 52,198.50

In Stock

Quantity

1

Base Price: ₹ 52,198.50

GST (18%): ₹ 9,395.73

Total Price: ₹ 61,594.23

Antigen

CANT1

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3

Gene Accession No.

Q8WVQ1

Gene Symbols

CANT1

Immunogen

Human recombinant protein fragment corresponding to amino acids 63-401 of CANT1 produced in E.coli

Quantity

100μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG1

Applications

Immunohistochemistry (Paraffin), Western Blot

Clone

OTI7F8

Conjugate

Unconjugated

Gene

CANT1

Gene Alias

5830420C20Rik; Apy1h; apyrase 1, homolog (C. lectularius); apyrase homolog; Ca2+-dependent endoplasmic reticulum nucleoside diphosphatase; calcium activated nucleotidase 1; Cant1; D11Bwg0554e; DBQD; DBQD1; EC 3.6.1.6; ectonucleoside triphosphate diphosphohydrolase 8; Entpd8; galectin-3-binding protein; soluble calcium-activated nucleotidase 1; lectin, galactoside-binding, soluble, 3 binding protein; LGALS3BP; micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification; putative MAPK-activating protein PM09; Putative NF-kappa-B-activating protein 107; SCAN1; SCAN-1; SHAPY; soluble Ca-activated nucleotidase, isozyme 1; soluble calcium-activated nucleotidase 1; soluble calcium-activated nucleotidase SCAN-1; srapy

Host Species

Mouse

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

124583

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • This protein encoded by this gene belongs to the apyrase family
  • It functions as a calcium-dependent nucleotidase with a preference for UDP
  • Mutations in this gene are associated with Desbuquois dysplasia with hand anomalies.