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GNL3 Monoclonal Antibody (2B9)

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Datasheet
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Datasheet
Protocols
Questions & Answers

Cite GNL3 Monoclonal Antibody (2B9)

  • Antibody Testing Data (1)
GNL3 Antibody in Western Blot (WB)
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GNL3 Antibody in Western Blot (WB)
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GNL3 Antibody (H00026354-M10) in WB

Western Blot analysis of GNL3 expression in transfected 293T cell line by GNL3 monoclonal antibody (M10), clone 2B9. Lane 1: GNL3 transfected lysate (Predicted MW: 62 KDa). Lane 2: Non-transfected lysate. . {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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GNL3 Antibody in Western Blot (WB)

Product Details

H00026354-M10

Applications
Tested Dilution
Publications

Western Blot (WB)

1-5 µg/mL
-

ELISA (ELISA)

10 µg/mL
-
Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG2a, kappa

Class

Monoclonal

Type

Antibody

Clone

2B9

Immunogen

GNL3 (AAH01024.1, 328 a.a. approximately 427 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

0.5 mg/mL

Purification

Protein A

Storage buffer

PBS, pH 7.4

Contains

no preservative

Storage conditions

-20°C, Avoid Freeze/Thaw Cycles

Shipping conditions

Wet ice

Product Specific Information

Product may be used with Western Blot (Transfected lysate).

Immunogen sequence: IEVVKPMEAA SAILSQADAR QVVLKYTVPG YRNSLEFFTM LAQRRGMHQK GGIPNVEGAA KLLWSEWTGA SLAYYCHPPT SWTPPPYFNE SIVVDMKSGF

Target Information

Arylsulfatase F, also known as ARSF, is a 590 amino acid secretory protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Arylsulfatase F uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition. The activity of Arylsulfatase F, unlike that of other family members, such as Arylsulfatase E, is not inhibited by warfarin. The gene encoding Arylsulfatase F maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: E2-induced gene 3 protein; estradiol-induced nucleotide binding protein; guanine nucleotide binding protein-like 3 (nucleolar); Guanine nucleotide-binding protein-like 3; MGC800; NNP47; Novel nucleolar protein 47; Nucleolar GTP-binding protein 3; Nucleostemin

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Gene Aliases: C77032; E2IG3; GNL3; NNP47; NS

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UniProt ID: (Human) Q9BVP2

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Entrez Gene ID: (Human) 26354

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Function(s)
GTPase activity protein binding GTP binding poly(A) RNA binding
Process(es)
cell proliferation positive regulation of telomere maintenance positive regulation of protein sumoylation regulation of cell proliferation ribosome biogenesis positive regulation of pri-miRNA transcription from RNA polymerase II promoter positive regulation of protein localization to chromosome, telomeric region
It has to be done as per old AB suggested Products section.
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If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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