跳转至内容
Merck
CN

SAB4200092

Anti-OSTF1 antibody, Mouse monoclonal

clone OSTF21, purified from hybridoma cell culture

别名:

Anti-OSF, Anti-Osteoclast-stimulating factor

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
OSTF21, monoclonal
Application:
IF, WB
Citations:
2
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


biological source

mouse

conjugate

unconjugated

antibody form

purified from hybridoma cell culture

antibody product type

primary antibodies

clone

OSTF21, monoclonal

form

buffered aqueous solution

mol wt

antigen ~28 kDa

species reactivity

rat, monkey, mouse, bovine, human

packaging

antibody small pack of 25 μL

concentration

~1.5 mg/mL

technique(s)

indirect immunofluorescence: 10-20 μg/mL using MCF-7 cells, western blot: 0.5-1 μg/mL using NRK cell extracts

isotype

IgG2b

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... OSTF1(26578)
mouse ... Ostf1(20409)
rat ... Ostf1(259275)

General description

Monoclonal Anti-OSTF1 (mouse IgG2b isotype) is derived from the hybridoma OSTF21 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide.The osteoclast-stimulating factor (OSF or OSTF1) contains a short proline-rich N-terminal region, an SH3 domain, three ankyrin repeats and an aspartate rich C-terminal region. It is a novel 28 kDa intracellular protein predominantly expressed in osteoclast (OCL). The OSTF1 gene is mapped to human chromosome 9q21.13.

Application

Anti-OSTF1 antibody, Mouse monoclonal is suitable for immunoblotting and immunofluorescence.

Biochem/physiol Actions

Monoclonal Anti-OSTF1 recognizes human, monkey, bovine, rat, and mouse OSTF1.
Osteoclast-stimulating factor (OSF or OSTF1) is potentially involved in protein-protein interactions. It supports bone resorption by cellular signal transduction cascade. OSTF1 induces osteoclast (OCL) bone formation by its SH3 domain interacting with spinal muscular atrophy disease determining gene product, survival motor neuron (SMN). The OSF SH3-SMN interaction might be significant in congenital bone fractures associated with type I spinal muscular atrophy disease. Repressed, OSF-SH3 domain interaction with its protein partners might cause reduced bone resorption by OCL. This prevents the bone loss that is associated with many bone diseases, such as osteoporosis, periodontal disease, Paget′s disease, estrogen deficiency, inflammatory bone loss, hyperparathyroidism and bone malignancy.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Preparation Note

Store at –20 °C. For continuous use, the product may be stored at 2–8 °C for up to one month. For extended storage, freeze in working aliquots at –20 °C. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.


Still not finding the right product?

试用我们的 产品选型工具 工具缩小选择范围


存储类别

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

新产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库


相关内容


Structure of the SH3 domain of human osteoclast-stimulating factor at atomic resolution
Chen L, et al.
Acta Crystallographica Section F, Structural Biology and Crystallization Communications, 62(9), 844-844 (2006)
RORB gene and 9q21. 13 microdeletion: report on a patient with epilepsy and mild intellectual disability
Baglietto MG, et al.
European Journal of Medical Genetics, 57(1), 44-46 (2014)



全球贸易项目编号

货号GTIN
SAB4200092-25UL04061837875359
SAB4200092-200UL04061836270568