PIMA532524

Dysferlin Recombinant Rabbit Monoclonal Antibody (JF05-54), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA532524-Each-of-1 In Stock ₹ 47,837.50

PIMA532524 - Each of 1

₹ 47,837.50

In Stock

Quantity

1

Base Price: ₹ 47,837.50

GST (18%): ₹ 8,610.75

Total Price: ₹ 56,448.25

Antigen

Dysferlin

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

TBS with 0.05% BSA, 40% Glycerol and 0.05% sodium azide, pH 7.4

Gene Accession No.

O75923, Q9ESD7

Gene Symbols

DYSF

Immunogen

Synthetic peptide within Human Dysferlin aa 113-162

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

Applications

Immunocytochemistry, Immunohistochemistry, Western Blot, Western Blot

Clone

JF05-54

Conjugate

Unconjugated

Gene

DYSF

Gene Alias

2310004N10Rik, AI604795, D6Pas3, Dysf, Dysferlin, dysferlin variant a, dysferlin_a, dystrophy-associated fer-1-like 1, dystrophy-associated fer-1-like protein, FER1L1, fer-1-like family member 1, fer-1-like protein 1, FLJ00175, FLJ90168, LGMD2B, limb girdle muscular dystrophy 2B (autosomal recessive), MMD1

Host Species

Rabbit

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

26903, 8291

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

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Description

  • Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems
  • The expression systems are developed by cloning in the specific antibody DNA sequences from immunoreactive rabbits
  • Then, individual clones are screened to select the best candidates for production
  • The advantages of using recombinant rabbit monoclonal antibodies include: better specificity and sensitivity, lot-to-lot consistency, animal origin-free formulations, and broader immunoreactivity to diverse targets due to larger rabbit immune repertoire
  • Dysferlin is the protein product of the 2p13 gene that is defective in patients with Limb-Girdle Muscular Dystrophy type 2B (LGMD2B) and Miyoshi Myopathy (MM)
  • Dysferlin is normally localized to the muscle plasma membrane
  • In patients with LGMD2B and MM, immunoreactivity to dysferlin is severely reduced or lost, depending on the type of mutation
  • This antibody is used for the characterization of LGMD2B and MM.