MA1724

GCAP1 Monoclonal Antibody (G2), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 MA1724-Each-of-1 In Stock ₹ 40,940.00

MA1724 - Each of 1

₹ 40,940.00

In Stock

Quantity

1

Base Price: ₹ 40,940.00

GST (18%): ₹ 7,369.20

Total Price: ₹ 48,309.20

Antigen

GCAP1

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with 1mg/mL BSA and 0.05% sodium azide

Gene Accession No.

P43080, P46065

Gene Symbols

Guca1a

Immunogen

Bacterial expressed full length GCAP-1.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Bovine, Human, Non-human Primate

Product Type

Antibody

Isotype

IgG2a

Applications

Western Blot

Clone

G2

Conjugate

Unconjugated

Gene

Guca1a

Gene Alias

C6orf131; COD3; cone dystrophy 3; CORD14; GC-A; GCAP; GCAP 1; GCAP1; Guanylate cyclase activator 1A; guanylate cyclase activator 1a (retina); guanylate cyclase-activating protein, photoreceptor 1; guanylin 1, retina; guanylyl cyclase-activating protein; guanylyl cyclase-activating protein 1; GUCA; GUCA1; GUCA1A; mGCAP1

Host Species

Mouse

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

282243, 2978

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • MA1-724 detects GCAP-1 from human, non-human primate and bovine samples
  • This antibody is specific for GCAP-1 and does not react with other isotypes
  • MA1-724 has been successfully used in Western blot procedures
  • By Western blot, this antibody detects a ∽23 kDa protein representing GCAP-1 protein on bovine rod outer segment membranes
  • The MA1-724 immunogen is bacterial expressed full length GCAP-1
  • Guanylate cyclase-activating protein is a l Ca(2+)-binding protein that upregulates synthesis of cGMP in photoreceptors
  • The known mammalian GCAPs are more than 90% similar, consisting of 201 to 205 amino acids, and containing 3 identically conserved Ca(2+)-binding sites
  • The GUCA1A gene, also termed GCAP1, is transcribed into a single 1.7-kb mRNA species detectable only in the retina
  • In a 4-generation British family with typical clinical features of autosomal dominant cone dystrophy a tyr99-to-cys mutation) in the GUCA1A gene has been identified
  • Another family with a pro50-to-leu mutation in GUCA1A demonstrated phenotypic variability ranging from mild photophobia to rod-cone dystrophy
  • The mutant protein could activate guanylate cyclase 1 (GUCY2D) and displayed similar calcium sensitivity to wildtype protein
  • However, there was a marked increase in the susceptibility to protease degradation and a reduction in the thermal stability of the pro50-to-leu mutation, which may depress cellular concentration and thereby contribute to retinal cell mortality.