Explore
Validate
LearnHPA041091
antibody from Atlas Antibodies
Targeting: DYNC2I2
bA216B9.3, CFAP133, DIC5, FAP133, MGC20486, WDR34
ImmunocytochemistryAntibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations [0]
Submit
Validation data
Reference
Comment
Report error
- Product number
- HPA041091 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA041091, RRID:AB_10796237
- Product name
- Anti-WDR34
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human WDR34, Gene description: WD repeat domain 34, Alternative Gene Names: bA216B9.3, DIC5, FAP133, MGC20486, Validated applications: ICC, IHC, Uniprot ID: Q96EX3, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.2 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling
Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome
Bosakova M, Abraham S, Nita A, Hruba E, Buchtova M, Taylor S, Duran I, Martin J, Svozilova K, Barta T, Varecha M, Balek L, Kohoutek J, Radaszkiewicz T, Pusapati G, Bryja V, Rush E, Thiffault I, Nickerson D, Bamshad M, Rohatgi R, Cohn D, Krakow D, Krejci P
EMBO Molecular Medicine 2020;12(11)
EMBO Molecular Medicine 2020;12(11)
Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome
Taylor S, Dantas T, Duran I, Wu S, Lachman R, Bamshad M, Shendure J, Nickerson D, Nelson S, Cohn D, Vallee R, Krakow D
Nature Communications 2015;6(1)
Nature Communications 2015;6(1)
No comments: Submit comment
No validations: Submit validation data