ANKH 产品
(Ankylosis, Progressive Homolog (Mouse) (ANKH))
Categories
This gene encodes a multipass transmembrane protein that is expressed in joints and other tissues and controls pyrophosphate levels in cultured cells. Progressive ankylosis-mediated control of pyrophosphate levels has been suggested as a possible mechanism regulating tissue calcification and susceptibility to arthritis in higher animals. Mutations in this gene have been associated with autosomal dominant craniometaphyseal dysplasia. [provided by RefSeq, Jul 2008].
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Featured ANKH Categories
Recommended ANKH 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human, Mouse
Application
WB, FACS, IHC (p)
Validations
- (4)
Cat. No.
ABIN653697
Quantity
400 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, IHC
Validations
- (2)
Cat. No.
ABIN7264924
Quantity
200 μL
Datasheet
Datasheet
Reactivity
Human, Mouse
Application
WB, IHC, FACS, IHC (p)
Validations
- (2)
Cat. No.
ABIN1892978
Quantity
200 μL
Datasheet
Datasheet
Recommended ANKH 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
Wheat germ
Validations
- (1)
Cat. No.
ABIN1345071
Quantity
10 μg
Datasheet
Datasheet
Reactivity
Human
Source
Tobacco (Nicotiana tabacum)
Validations
- (1)
Cat. No.
ABIN3107094
Quantity
1 mg
Datasheet
Datasheet
Reactivity
Human
Source
Escherichia coli (E. coli)
Validations
- (1)
Cat. No.
ABIN3089124
Quantity
1 mg
Datasheet
Datasheet
Latest Publications for our ANKH Products
: "Familial calcium pyrophosphate dihydrate deposition disease and the ANKH gene." in: Current opinion in rheumatology, Vol. 15, Issue 3, pp. 326-31, (2003) (PubMed).: "The program of androgen-responsive genes in neoplastic prostate epithelium." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 99, Issue 18, pp. 11890-5, (2002) (PubMed).
: "Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH." in: American journal of human genetics, Vol. 71, Issue 4, pp. 985-91, (2002) (PubMed).
: "Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK." in: American journal of human genetics, Vol. 68, Issue 6, pp. 1321-6, (2001) (PubMed).
: "Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia." in: Nature genetics, Vol. 28, Issue 1, pp. 37-41, (2001) (PubMed).
: "Role of the mouse ank gene in control of tissue calcification and arthritis." in: Science (New York, N.Y.), Vol. 289, Issue 5477, pp. 265-70, (2000) (PubMed).
Synonyms and alternative names related to ANKH
ANKH inorganic pyrophosphate transport regulator (ANKH), ANKH inorganic pyrophosphate transport regulator (Ankh), progressive ankylosis (Ank), ANKH inorganic pyrophosphate transport regulator b (ankhb), ANKH inorganic pyrophosphate transport regulator S homeolog (ankh.S), ANKH inorganic pyrophosphate transport regulator a (ankha), ANK, Ank, ank, Ankh, ankh, CCAL2, CMDJ, CPPDD, D15Ertd221e, HANK, MANK, mKIAA1581, wu:fc08d03, wu:fj64g09, zgc:110290Protein level used designations for ANKH
- ankylosis, progressive homolog
- progressive ankylosis protein homolog
- progressive ankylosis homolog
- progressive ankylosis protein
- ankylosis, progressive homolog (mouse)
- progressive ankylosis protein homolog-like
- fn54 protein
- ANK-B
- progressive ankylosis protein homolog B
- progressive ankylosis-like protein
- ankylosis, progressive homolog a
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