Protein FAM111B Antibodies

AND FAM111B ELISA kits, Protein FAM111B Proteins

Many biological assays use antibodies to detect Protein FAM111B, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Protein FAM111B in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Protein FAM111B antibodies...

We validate the specificity of these antibodies to Protein FAM111B by testing them on tissues known to express FAM111B positively and negatively. Browse below to find the FAM111B antibody that suites your experiment. We have 3 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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FAM111B Infographic by Boster Bio

All FAM111B Products

Product

Figures

Specificity

Applications

Price

Anti-Protein FAM111B FAM111B Antibody

Human

ELISA, IHC

$380
Cat # A14246
100ul

FAM111B (NM_198947) Human Over-expression Lysate

Human

$960
Cat # LS374393
100 µg

Anti-FAM111B Antibody Picoband™

Human

ELISA, Flow Cytometry, IHC, WB

$370
Cat # A14246-2
100 μg/vial

FAM111B Overview

Facts about Protein FAM111B.

Protein FAM111B (FAM111B)

Gene Information

Human
Gene Name:	FAM111B
Uniprot:	Q6SJ93
Entrez:	374393

Family

Belongs to:

FAM111 family

Alternative Names

family with sequence similarity 111, member B

Molecular Weight

Mass (kDA):
84.674 kDA

Genomic Context


Human

Location:	11q12.1
Sequence:	11; NC_000011.10 (59107185..59127415)

Tissue Specificity

Widely expressed.

Diseases

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP)

Interacting Proteins

PTMs

Acetylation

Isopeptide bond

Ubl conjugation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/FAM111B

References

PMID: 24268661 by Mercier S., et al. Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis.