Gem Nuclear Organelle Associated Protein 2 (GEMIN2) Antibody

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195€ (20 µl)

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935106861
info@markelab.com
name
Gem Nuclear Organelle Associated Protein 2 (GEMIN2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx002220
tested applications
ELISA, WB, IHC

Description

GEMIN2 Antibody is a Rabbit Polyclonal antibody against GEMIN2. This gene encodes one of the proteins found in the SMN complex, which consists of several gemin proteins and the protein known as the survival of motor neuron protein. The SMN complex is localized to a subnuclear compartment called gems (gemini of coiled bodies) and is required for assembly of spliceosomal snRNPs and for pre-mRNA splicing. This protein interacts directly with the survival of motor neuron protein and it is required for formation of the SMN complex. A knockout mouse targeting the mouse homolog of this gene exhibited disrupted snRNP assembly and motor neuron degeneration.

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Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Gem Nuclear Organelle Associated Protein 2 (GEMIN2)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
ELISA: 1 µg/ml, WB: 1/500 - 1/1000, IHC-P: 1/50 - 1/200. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
O14893
Gene ID
8487
NCBI Accession
NP_003607.1
Background
Antibody anti-GEMIN2
Status
RUO
Note
Concentration: > 0.2 mg/ml -

Descripción

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GEMIN2 Antibody is a Rabbit Polyclonal antibody against GEMIN2. This gene encodes one of the proteins found in the SMN complex, which consists of several gemin proteins and the protein known as the survival of motor neuron protein. The SMN complex is localized to a subnuclear compartment called gems (gemini of coiled bodies) and is required for assembly of spliceosomal snRNPs and for pre-mRNA splicing. This protein interacts directly with the survival of motor neuron protein and it is required for formation of the SMN complex. A knockout mouse targeting the mouse homolog of this gene exhibited disrupted snRNP assembly and motor neuron degeneration.

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