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Polyclonal Anti-IHH

Cat no: PA2225

Polyclonal Anti-IHH

Rabbit IgG polyclonal antibody for Indian hedgehog protein (IHH) detection. Tested with WB in Human;Mouse;Rat.

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SPECIFICATIONS

Price

200.00 USD

Catalog Number

PA2225

Size

100?g/vial

Applications

WB

Reactivities

Hum, Mouse, Rat

Form

lyophilized

Format

Each vial contains 5mg BSA, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg Thimerosal, 0.05mg NaN3.

Gene Id

IHH

References

1. Berman, D. M., Karhadkar, S. S., Maitra, A., Montes de Oca, R., Gerstenblith, M. R., Briggs, K., Parker, A. R., Shimada, Y., Eshleman, J. R., Watkins, D. N., Beachy, P. A. Widespread requirement for hedgehog ligand stimulation in growth of digestive tract tumours. Nature 425: 846-851, 2003. \n2. Chung, U., Schipani, E., McMahon, A. P., Kronenberg, H. M. Indian hedgehog couples chondrogenesis to osteogenesis in endochondral bone development. J. Clin. Invest. 107: 295-304, 2001.\n3. Giordano, N., Gennari, L., Bruttini, M., Mari, F., Meloni, I., Baldi, C., Capoccia, S., Geraci, S., Merlotti, D., Amendola, A., Martini, G., Nuti, R., Gennari, C., Renieri, A. Mild brachydactyly type A1 maps to chromosome 2q35-q36 and is caused by a novel IHH mutation in a three generation family. J. Med. Genet. 40: 132-135, 2003.\n

Swiss Prot

Q14623

Storage Temp

At -20 degree C for one year. After reconstitution, at 4 degree C for one month. It can also be aliquotted and stored frozen at -20 degree C for a longer time.Avoid repeated freezing and thawing.

Additional Info

A synthetic peptide corresponding to a sequence at the C-terminus of human IHH, different from the related mouse and rat sequences by one amino acid.

Scientific Background

Indian hedgehog, also known as IHH or HHG2 is a protein which in humans is encoded by the IHH gene. This gene encodes a member of the hedgehog family of secreted signaling molecules. IHH gene is mapped to 2q35. Hedgehog proteins are essential regulators of a variety of developmental processes including growth, patterning and morphogenesis. The encoded protein specifically plays a role in bone growth a differentiation. Mutations in this gene are the cause of brachydactyly type A1 which is characterized by shortening or malformation of the phalanges. Mutations in this gene are also the cause of acrocapitofemoral dysplasia.

SUPPLIER INFO

Boster Immunoleader

Applications

WB

Reactivities

Hum

More info

Applications

ELISA, WB

Reactivities

Hum

More info

Applications

ELISA, IHC, WB

Reactivities

Hum

More info

Applications

ELISA, WB

Reactivities

Mouse

More info

Applications

ELISA, IHC, WB

Reactivities

Rat

More info

Applications

BNI, ELISA, IHC, IP, WB

Reactivities

Mouse

Conjugates

Unconj, Agarose, AP, Biotin, Gold, HRP, BE, GE, YE, OE, RE, FRE, NIR, ONFC

More info

Applications

BNI, ELISA, IHC, IP, WB

Reactivities

Rat

More info

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