Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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- Product number
- ABIN1673359 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Discoidin Domain Receptor tyrosine Kinase 2 (DDR2) (C-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- A synthetic peptide corresponding to a sequence at the C-terminal of human DDR2, different from the related mouse sequence by three amino acids.Immunogen affinity purified.
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- C-Term
- Isotype
- IgG
- Vial size
- 100 μg
- Storage
- At -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Mutations in DDR2 gene cause SMED with short limbs and abnormal calcifications.
The collagen receptor DDR2 regulates proliferation and its elimination leads to dwarfism.
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.
Bargal R, Cormier-Daire V, Ben-Neriah Z, Le Merrer M, Sosna J, Melki J, Zangen DH, Smithson SF, Borochowitz Z, Belostotsky R, Raas-Rothschild A
American journal of human genetics 2009 Jan;84(1):80-4
American journal of human genetics 2009 Jan;84(1):80-4
The collagen receptor DDR2 regulates proliferation and its elimination leads to dwarfism.
Labrador JP, Azcoitia V, Tuckermann J, Lin C, Olaso E, Mañes S, Brückner K, Goergen JL, Lemke G, Yancopoulos G, Angel P, Martínez C, Klein R
EMBO reports 2001 May;2(5):446-52
EMBO reports 2001 May;2(5):446-52
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.
Borochowitz Z, Langer LO Jr, Gruber HE, Lachman R, Katznelson MB, Rimoin DL
American journal of medical genetics 1993 Feb 1;45(3):320-6
American journal of medical genetics 1993 Feb 1;45(3):320-6
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