B9D1 Antibody

Code CSB-PA892487ESR2HU
Size US$166
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  • Immunohistochemistry of paraffin-embedded human liver tissue using CSB-PA892487ESR2HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) B9D1 Polyclonal antibody
Uniprot No.
Target Names
B9D1
Alternative Names
B9D1 antibody; MKSR1B9 domain-containing protein 1 antibody; MKS1-related protein 1 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human B9 domain-containing protein 1 protein (1-130AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Tested Applications
ELISA, IHC
Recommended Dilution
Application Recommended Dilution
IHC 1:20-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
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. Required for ciliogenesis and sonic hedgehog/SHH signaling.
Gene References into Functions
  1. describe four patients with mild Joubert phenotypes who carry pathogenic mutations in either MKS1 or B9D1, two genes previously implicated only in Meckel syndrome PMID: 24886560
  2. B9D1 is a novel Meckel syndrome gene PMID: 21493627
  3. Ciliary transition zone localization. Functions in a module with related proteins (MKS1 and B9D1) that cooperates with nephrocystins in ciliogenesis. PMID: 18337471
  4. MKS-1 and MKS-1-related proteins 1 and 2 (MKSR-1/EPPB9, MKSR-2/B9D2), localize to transition zones/basal bodies of sensory cilia; subcellular localization is largely co-dependent, pointing to a functional relationship between the proteins PMID: 19208769
Involvement in disease
Meckel syndrome 9 (MKS9); Joubert syndrome 27 (JBTS27)
Subcellular Location
Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, cilium axoneme.
Protein Families
B9D family
Database Links

HGNC: 24123

OMIM: 614144

KEGG: hsa:27077

STRING: 9606.ENSP00000261499

UniGene: Hs.309467

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7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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