PIMA525373

LMAN1 Monoclonal Antibody (OTI1C5), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA525373-Each-of-1 In Stock ₹ 55,447.00

PIMA525373 - Each of 1

₹ 55,447.00

In Stock

Quantity

1

Base Price: ₹ 55,447.00

GST (18%): ₹ 9,980.46

Total Price: ₹ 65,427.46

Antigen

LMAN1

Classification

Monoclonal

Concentration

1.0 mg/mL

Formulation

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

Gene Accession No.

P49257

Gene Symbols

LMAN1

Immunogen

Full length human recombinant protein of LMAN1 produced in HEK293T cell

Quantity

100μL

Primary or Secondary

Primary

Target Species

Human, Non-human Primate

Product Type

Antibody

Isotype

IgG1

Applications

Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Clone

OTI1C5

Conjugate

Unconjugated

Gene

LMAN1

Gene Alias

2610020P13Rik; AI326273; AU043785; C730041J05; EGK_09725; endoplasmic reticulum-golgi intermediate compartment protein 53; ERGIC53; ERGIC-53; ER-Golgi intermediate compartment 53 kDa protein; F5F8D; FMFD1; Gp58; intracellular mannose-specific lectin MR60; Lectin mannose-binding 1; lectin, mannose binding 1; lectin, mannose-binding, 1; LMAN1; MCFD1; MR60; P58; Protein ERGIC-53

Host Species

Mouse

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

3998

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments
  • The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells
  • Mutations in the gene are associated with a coagulation defect
  • Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.