Cell Biology Antibodies 10
Anti-IHH Antibody (CAB6626)
- SKU:
- CAB6626
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Description
Antibody Name: | Anti-IHH Antibody |
Antibody SKU: | CAB6626 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 202-411 of human IHH (NP_002172.2). |
Application: | WB |
Recommended Dilution: | WB 1:500 - 1:2000 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | Human placenta, Mouse kidney, Mouse liver, Mouse ovary, Rat liver, Rat lung, Rat brain |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 202-411 of human IHH (NP_002172.2). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | GCFP AGAQ VRLE SGAR VALS AVRP GDRV LAMG EDGS PTFS DVLI FLDR EPHR LRAF QVIE TQDP PRRL ALTP AHLL FTAD NHTE PAAR FRAT FASH VQPG QYVL VAGV PGLQ PARV AAVS THVA LGAY APLT KHGT LVVE DVVA SCFA AVAD HHLA QLAF WPLR LFHS LAWG SWTP GEGV HWYP QLLY RLGR LLLE EGSF HPLG MSGA GS |
Gene ID: | 3549 |
Uniprot: | Q14623 |
Cellular Location: | Cell membrane, Extracellular side, Lipid-anchor, Secreted, extracellular space |
Calculated MW: | 45kDa |
Observed MW: | 53kDa |
Synonyms: | IHH, BDA1, HHG2 |
Background: | This gene encodes a member of the hedgehog family of proteins. The encoded preproprotein is proteolytically processed to generate multiple protein products, including an N-terminal fragment that is involved in signaling. Hedgehog family proteins are essential secreted signaling molecules that regulate a variety of developmental processes including growth, patterning and morphogenesis. The protein encoded by this gene specifically plays a role in bone growth and differentiation. Mutations in this gene are the cause of brachydactyly type A1, which is characterized by shortening or malformation of the fingers and toes. Mutations in this gene are also the cause of acrocapitofemoral dysplasia. |
UniProt Protein Function: | IHH: Intercellular signal essential for a variety of patterning events during development. Binds to the patched (PTC) receptor, which functions in association with smoothened (SMO), to activate the transcription of target genes. Implicated in endochondral ossification: may regulate the balance between growth and ossification of the developing bones. Induces the expression of parathyroid hormone-related protein (PTHRP). Expressed in embryonic lung, and in adult kidney and liver. Belongs to the hedgehog family. |
UniProt Protein Details: | Chromosomal Location of Human Ortholog: 2q33-q35 Cellular Component: extracellular matrix; extracellular space; plasma membrane Molecular Function:peptidase activity; patched binding; calcium ion binding Biological Process: vitelline membrane formation; proteoglycan metabolic process; maternal process involved in pregnancy; cell maturation; positive regulation of collagen biosynthetic process; cell fate specification; proteolysis; embryonic pattern specification; response to estradiol stimulus; positive regulation of T cell differentiation in the thymus; smooth muscle development; cell-cell signaling; embryonic digestive tract morphogenesis; regulation of growth; pancreas development; positive regulation of mesenchymal cell proliferation; positive regulation of smoothened signaling pathway; heart looping; skeletal development; bone resorption; negative regulation of immature T cell proliferation in the thymus; smoothened signaling pathway; intein-mediated protein splicing; in utero embryonic development; multicellular organism growth; negative regulation of eye pigmentation; negative regulation of T cell differentiation in the thymus; negative regulation of signal transduction; patterning of blood vessels; osteoblast differentiation; positive regulation of chondrocyte differentiation; cartilage development; neuron development; positive regulation of transcription from RNA polymerase II promoter; embryonic digit morphogenesis; embryonic camera-type eye morphogenesis; positive regulation of alpha-beta T cell differentiation; positive regulation of epithelial cell proliferation; negative regulation of apoptosis; negative regulation of alpha-beta T cell differentiation Disease: Brachydactyly, Type A1; Acrocapitofemoral Dysplasia |
NCBI Summary: | This gene 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. [provided by RefSeq, Feb 2010] |
UniProt Code: | Q14623 |
NCBI GenInfo Identifier: | 33112634 |
NCBI Gene ID: | 3549 |
NCBI Accession: | Q14623.4 |
UniProt Secondary Accession: | Q14623,O43322, Q8N4B9, B9EGM5, |
UniProt Related Accession: | Q14623 |
Molecular Weight: | 45,251 Da |
NCBI Full Name: | Indian hedgehog protein |
NCBI Synonym Full Names: | indian hedgehog |
NCBI Official Symbol: | IHH |
NCBI Official Synonym Symbols: | BDA1; HHG2 |
NCBI Protein Information: | indian hedgehog protein; HHG-2; Indian hedgehog homolog |
UniProt Protein Name: | Indian hedgehog protein |
UniProt Synonym Protein Names: | HHG-2Cleaved into the following 2 chains:Indian hedgehog protein N-product; Indian hedgehog protein C-product |
Protein Family: | Indian hedgehog protein |
UniProt Gene Name: | IHH |
UniProt Entry Name: | IHH_HUMAN |