B9D2 Antibodies

AND B9D2 ELISA kits, B9D2 Proteins

Many biological assays use antibodies to detect B9D2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with B9D2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop B9D2 antibodies...

We validate the specificity of these antibodies to B9D2 by testing them on tissues known to express B9D2 positively and negatively. Browse below to find the B9D2 antibody that suites your experiment. We have 2 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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B9D2 Infographic by Boster Bio

All B9D2 Products

Product

Figures

Specificity

Applications

Price

Human B9D2 Recombinant Protein

SDS-PAGE

$250
Cat # PROTQ9BPU9
Starting from 4ug

B9D2 (NM_030578) Human Over-expression Lysate

Human

$628
Cat # LS080776
100 µg

B9D2 Overview

Facts about B9 domain-containing protein 2.

B9D2 3D structure. Source: alphafold

B9 domain-containing protein 2 (B9D2)

Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. .

Gene Information

Human
Gene Name:	B9D2
Uniprot:	Q9BPU9
Entrez:	80776

Family

Belongs to:

B9D family

Alternative Names

B9 domain-containing protein 2; B9 protein domain 2; ICIS-1; involved in cIlia stability-1; MGC4093; MKS1-related protein 2; MKSR2

Molecular Weight

Mass (kDA):
19.261 kDA

Genomic Context


Human

Location:	19q13.2
Sequence:	19; NC_000019.10 (41354417..41364534, complement)

Subcellular Localizations

Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, cilium axoneme. Nucleus.

Diseases

Meckel-gruber Syndrome
Familial Aplasia Of The Vermis
Cystic Kidney Diseases
Cerebellar Diseases
Polydactyly
Bardet-biedl Syndrome
Congenital Cerebral Hernia
Eye Abnormalities
Nephronophthisis
Occipital Encephalocele

Ciliary Motility Disorders
Polycystic Kidney Diseases
Kidney Diseases
Simple Renal Cyst

Interacting Proteins

INVS
TTC30B

Pathways

Localization
Transport
Gastrulation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/B9D2

References

PMID: 19208769 by Bialas N.J., et al. Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins.

PMID: 21763481 by Dowdle W.E., et al. Disruption of a ciliary B9 protein complex causes Meckel syndrome.