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BMP-1, Polyclonal Antibody

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产品名称: BMP-1, Polyclonal Antibody
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简单介绍

BMP-1, Polyclonal Antibody


BMP-1, Polyclonal Antibody  的详细介绍
Product Name

BMP-1, Polyclonal Antibody

Full Product Name

BMP-1 Polyclonal Antibody

Product Synonym Names
Bone morphogenetic protein 1 (BMP-1) (EC 3.4.24.19) (Mammalian tolloid protein) (mTld) (Procollagen C-proteinase) (PCP)
Product Gene Name

anti-BMP-1 antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
U50330 mRNA
3D Structure
ModBase 3D Structure for P13497
Clonality
Polyclonal
Host
Rabbit
Species Reactivity
Human, Mouse, Rat
Specificity
The antibody detects endogenous BMP-1
Purity/Purification
Affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Form/Format
PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.
Concentration
1 mg/ml (lot specific)
Immunogen
Synthetic peptide from human protein at AA range: 131-180
Immunogen Type
Protein
Preparation and Storage
Store at -20 degree C
Other Notes
Small volumes of anti-BMP-1 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.
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Product Categories/Family for anti-BMP-1 antibody
Total protein Ab
Applications Tested/Suitable for anti-BMP-1 antibody
Immunohistochemistry (IHC)
Application Notes for anti-BMP-1 antibody
IHC: 1:50-300

Immunohistochemistry (IHC) of anti-BMP-1 antibody
Immunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:200
anti-BMP-1 antibody Immunohistochemistry (IHC) (IHC) image
Immunohistochemistry (IHC) of anti-BMP-1 antibody
Immunohistochemical analysis of paraffin-embedded human-skin, antibody was diluted at 1:200
anti-BMP-1 antibody Immunohistochemistry (IHC) (IHC) image
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NCBI/Uniprot data below describe general gene information for BMP-1. It may not necessarily be applicable to this product.
NCBI GI #
4502421
NCBI GeneID
649
NCBI Accession #
NP_001190.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001199.3 [Other Products]
UniProt Primary Accession #
P13497 [Other Products]
UniProt Secondary Accession #
Q13292; Q13872; Q14874; Q99421; Q99422; Q99423; Q9UL38; A8K6F5; B2RN46; D3DSR0[Other Products]
UniProt Related Accession #
P13497[Other Products]
Molecular Weight
92,655 Da
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NCBI Official Full Name
bone morphogenetic protein 1 isoform 1
NCBI Official Synonym Full Names
bone morphogenetic protein 1
NCBI Official Symbol
BMP1  [Similar Products]
NCBI Official Synonym Symbols
PCP; TLD; OI13; PCP2; PCOLC
  [Similar Products]
NCBI Protein Information
bone morphogenetic protein 1
UniProt Protein Name
Bone morphogenetic protein 1
UniProt Synonym Protein Names
Mammalian tolloid protein; mTld; Procollagen C-proteinase; PCP
UniProt Gene Name
BMP1  [Similar Products]
UniProt Synonym Gene Names
PCOLC; BMP-1; mTld; PCP  [Similar Products]
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NCBI Summary for BMP-1
This gene encodes a protein that is capable of inducing formation of cartilage in vivo. Although other bone morphogenetic proteins are members of the TGF-beta superfamily, this gene encodes a protein that is not closely related to other known growth factors. This gene is expressed as alternatively spliced variants that share an N-terminal protease domain but differ in their C-terminal region. [provided by RefSeq, Aug 2008]
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UniProt Comments for BMP-1
BMP1: Cleaves the C-terminal propeptides of procollagen I, II and III. Induces cartilage and bone formation. May participate in dorsoventral patterning during early development by cleaving chordin (CHRD). Defects in BMP1 are a cause of autosomal recessive osteogenesis imperfecta (AR-OI). A connective tissue disorder characterized by bone fragility, progressively deforming bones, bowing of limbs due to multiple fractures, very short stature, a triangular face, severe scoliosis, and grayish sclera. AR-OI due to BMP1 mutations belongs to the group of osteogenesis imperfecta type III in the Sillence classification. Belongs to the peptidase M12A family. 7 isoforms of the human protein are produced by alternative splicing.

Protein type: Cytokine; EC 3.4.24.19; Protease

Chromosomal Location of Human Ortholog: 8p21.3

Cellular Component: extracellular region

Molecular Function: metalloendopeptidase activity; peptidase activity; protein binding; serine-type endopeptidase activity

Biological Process: cartilage condensation; extracellular matrix disassembly; multicellular organismal development; proteolysis

Disease: Osteogenesis Imperfecta, Type Xiii
Research Articles on BMP-1
1. a previously unknown O-glycosylation site and Asn-hydroxylation site, indicating a novel feature of BMP-1 in the EGF domain. The study clearly outlines the benefit of in-depth characterization of overexpressed proteins to deduce important protein modifications.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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