ANKH, Polyclonal Antibody

Rabbit Polyclonal to Human ANKH; Human ANKH; CMDJ; CPPDD; HANK; KIAA1581; ANK; MANK; CCAL2

For Research Use Only. Not for use in diagnostic procedures.

Polyclonal

Rabbit

Human ANKH

Immunoaffinity purified

PBS, 0.09% sodium azide

Maintain refrigerated at 2-8 degree C for up to 6 months.
For long term storage store at -20 degree C.

Small volumes of anti-ANKH antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

ANKH Antibody, CMDJ Antibody, CPPDD Antibody, HANK Antibody, KIAA1581 Antibody, ANK Antibody, MANK Antibody, CCAL2 Antibody Description: ANKH is 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.

Immunohistochemistry (IHC) Paraffin, Western Blot (WB), Flow Cytometry (FC/FACS)

Flow Cytometry (1:10 - 1:50)
IHC-P (1:10 - 1:100)
WB (1:1000)

Anti-ANKH / ANK antibody IHC staining of human brain, cortex. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.

Western blot of ANKH Antibody in mouse cerebellum tissue lysates (35 ug/lane). ANKH (arrow) was detected using the purified antibody.

ANKH Antibody flow cytometry of K562 cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

32,259 Da

ANKH inorganic pyrophosphate transport regulator

progressive ankylosis protein homolog

Progressive ankylosis protein homolog

KIAA1581; ANK  [Similar Products]

ANKH_HUMAN

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]

ANKH: Regulates intra- and extracellular levels of inorganic pyrophosphate (PPi), probably functioning as PPi transporter. Defects in ANKH are the cause of chondrocalcinosis 2 (CCAL2). Chondrocalcinosis is a common cause of joint pain and arthritis caused by calcium deposition in articular cartilage and the presence of calcium hypophosphate crystals in synovial fluid, cartilage and periarticular soft tissue. CCAL2 inheritance is autosomal dominant. Defects in ANKH are the cause of craniometaphyseal dysplasia Jackson type (CMDJ). CMDJ is a rare autosomal dominant skeletal disorder characterized by abnormal bone formation and mineralization in membranous as well as endochondral bones. Progressive thickening of the bones can cause narrowing of cranial foramina and can lead to severe visual and neurological impairment, such as facial palsy and deafness. Belongs to the ANKH family.

Protein type: Membrane protein, multi-pass; Transporter; Membrane protein, integral

Chromosomal Location of Human Ortholog: 5p15.1

Cellular Component: integral to membrane; integral to plasma membrane; outer membrane; plasma membrane

Molecular Function: inorganic diphosphate transmembrane transporter activity; inorganic phosphate transmembrane transporter activity; phosphate transmembrane transporter activity

Biological Process: inorganic diphosphate transport; locomotory behavior; regulation of bone mineralization; skeletal development; transmembrane transport

Disease: Chondrocalcinosis 2; Craniometaphyseal Dysplasia, Autosomal Dominant

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