Thermo Fisher Scientific IHH Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

1:500-1:1,000

-

ELISA (ELISA)

1 µg/mL

-

Product Specifications

Species Reactivity

Human, Mouse, Rat

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 202-411 of human IHH (NP_0021722) if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:IHH,uniProtId:Q14623-1,ncbiNodeId:9606,antigenRange:202-411,antigenLength:411,antigenImageFileName:PA5-93107_IHH_Q14623-1_Rabbit.svg,antigenImageFileNamePDP:PA5-93107_IHH_Q14623-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

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Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1.51 mg/mL

Purification

Affinity Chromatography

Storage buffer

PBS, pH 7.3, with 50% glycerol

Contains

0.02% sodium azide

Storage conditions

-20° C, Avoid Freeze/Thaw Cycles

Shipping conditions

Wet ice

RRID

AB_2806627

Product Specific Information

Immunogen sequence: GCFPAGAQVR LESGARVALS AVRPGDRVLA MGEDGSPTFS DVLIFLDREP HRLRAFQVIE TQDPPRRLAL TPAHLLFTAD NHTEPAARFR ATFASHVQPG QYVLVAGVPG LQPARVAAVS THVALGAYAP LTKHGTLVVE DVVASCFAAV ADHHLAQLAF WPLRLFHSLA WGSWTPGEGV HWYPQLLYRL GRLLLEEGSF HPLGMSGAGS; Positive Samples: Human placenta, Mouse kidney, Mouse liver, Mouse ovary, Rat liver, Rat lung, Rat brain; Cellular Location: Cell membrane, Extracellular side, Lipid-anchor, extracellular space

Target Information

Ihh encodes a member of the hedgehog family of secreted signaling molecules. 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 an 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.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.