Rabbit polyclonal NYX antibody (A7830)

$69.00$259.00

Reactivity: Human,Mouse
Applications: WB,IHC
Conjugation: Unconjugated
Supplier: ABclonal Inc.

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Rabbit polyclonal NYX antibody (A7830)

Supplier: ABclonal Inc.

Recommended applications: WB,IHC

Recommended dilution:

WB 1:500 – 1:2000 IHC 1:50 – 1:100

Recommended protocols: check protocols

Image descriptions:

Click or hover above images to see image description for Rabbit polyclonal NYX antibody.

Alternative names:

Check alternative names for the antibody

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CLRP antibody, NBM1 antibody, CSNB1 antibody, CSNB4 antibody, CSNB1A antibody
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SCBT cat No:

Name

Rabbit polyclonal NYX antibody

Catalogue No.

A7830

Reactivity

Human, Mouse

Immunogen

Recombinant protein of human NYX

Host

Rabbit

Applications

WB, IHC

Recommended dilution

WB 1:500 – 1:2000
IHC 1:50 – 1:100

Clonality

Polyclonal

Conjugation

Unconjugated

Isotype

IgG

Molecular weight

Predicted: 52kDa/Observed: Refer to figures

Formulation

NYX antibody was tube-contained.
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Purification

NYX antibody was purified using affinity purification.

Storage

Store at -20 Celsius degree. Avoid freeze / thaw cycles.

Alternative antibody names

CLRP antibody, NBM1 antibody, CSNB1 antibody, CSNB4 antibody, CSNB1A antibody

Database links

Human UniProt/Swiss-Prot:Q9GZU5

Protein names

CLRP, NBM1, CSNB1, CSNB4, CSNB1A

Protein tissue specificity

Expressed in kidney and retina. Also at low levels in brain, testis and muscle. Within the retina, expressed in the inner segment of photoreceptors, outer and inner nuclear layers and the ganglion cell layer.

Protein sequence and domain

Belongs to the small leucine-rich proteoglycan (SLRP) family. SLRP class IV subfamily.; Contains 11 LRR (leucine-rich) repeats.; Contains 1 LRRCT domain.; Contains 1 LRRNT domain.

Protein cellular localization

Secreted, extracellular space, extracellular matrix .

Background

The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB.

Note

AntibodyPlus can customize NYX antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provides antibody trial sample for your own antibody validation.

Product type

Primary antibody

Supplier

ABclonal Inc.

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