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Catalog Number: (10154-746)
Supplier: Proteintech
Description: The DNTT,TDT Antibody from Proteintech is a rabbit polyclonal Antibody to a fusion protein of human DNTT,TDT. This Antibody recognizes human Antigen. The DNTT,TDT Antibody has been validated for the following applications: ELISA, IHC analysis.


Catalog Number: (76075-264)
Supplier: Prosci
Description: For WB starting dilution is: 1:1000 For IHC-P starting dilution is: 1:50~100 For FACS starting dilution is: 1:10~50


Catalog Number: (10475-970)
Supplier: Bioss
Description: Involved in vesicular transport in the osteoclast (By similarity). May have a role in sialyl-lex-mediated transduction of apoptotic signals.Tissue specificity: Expressed in placenta, liver, prostate, thymus, spleen, ovary, colon, colon carcinoma and peripheral blood lymphocytes (PBL). Weakly expressed in brain, lung, kidney, and testis. No expression in heart, skeletal muscle, pancreas and small intestine. Predominantly expressed in the breast carcinoma cell line MCF-7.Involvement in disease:Defects in PLEKHM1 are the cause of osteopetrosis autosomal recessive type 6 (OPTB6); also known as autosomal recessive osteopetrosis intermediate form. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or adulthood. Autosomal recessive osteopetrosis is usually associated with normal or elevated amount of non-functional osteoclasts.


Catalog Number: (89517-564)
Supplier: Abgent
Description: Western Blot: 1:1000


Catalog Number: (103259-572)
Supplier: Novus Biologicals
Description: The C6orf162 Antibody from Novus Biologicals is a rabbit polyclonal antibody to C6orf162. This antibody reacts with human. The C6orf162 Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.


Catalog Number: (76066-434)
Supplier: Prosci
Description: For WB starting dilution is: 1:1000 For IHC-P starting dilution is: 1:10~50


Catalog Number: (76171-158)
Supplier: Boster Biological Technology
Description: Rabbit IgG polyclonal antibody for Oxidized low-density lipoprotein receptor 1(OLR1) detection. Tested with WB in Human.


Catalog Number: (10791-588)
Supplier: Thermo Scientific
Description: The Thermo Scientific Cimarec+™ series of digital magnetic hotplate stirrers are designed to provide precise stirring control, exceptional safety, and temperature performance for routine protocols

CSA Certified


Catalog Number: (10207-296)
Supplier: Boster Biological Technology
Description: Rabbit IgG polyclonal antibody for Transcription factor E2F6(E2F6) detection. Tested with WB in Human;Mouse;Rat.


Catalog Number: (89514-722)
Supplier: Abgent
Description: Western Blot: 1:1000


Supplier: TCI America
Description: CAS Number: 6358-09-4 MDL Number: MFCD00035767 Molecular Formula: C6H5ClN2O3 Molecular Weight: 188.57 Purity/Analysis Method: <gt/>98.0% (T) Form: Crystal Melting point (°C): 162
Supplier: BeanTown Chemical
Description: CAS: 22059-21-8; EC No: 217-162-5; MDL No: MFCD00009944; RTECS: GZ1110000 Crystalline/Powder; Molecular Formula: C4H7NO2 ; MW: 101.10 Melting Point: 229-231°

SDS

Catalog Number: (10085-998)
Supplier: Proteintech
Description: DNAJC11 is a member of the J proteins also known as HSP40 family of co-chaperones. Recently DNAJC11 has been found to interact with mitofilin, a mitochondrial inner membrane protein, indicating that it may be a molecular chaperone during mitochondrial protein import and folding.


Supplier: BeanTown Chemical
Description: CAS: 631-61-8; EC No: 211-162-9; MDL No: MFCD00013066; RTECS: AF3675000 Crystalline; Linear Formula: CH3CO2NH4; MW: 77.08 Melting Point: 110-112° (decomposes) Hygroscopic

SDS

Catalog Number: (10308-482)
Supplier: Bioss
Description: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf162 gene product has been provisionally designated C1orf162 pending further characterization.


Catalog Number: (10279-410)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf32 gene product has been provisionally designated C6orf32 pending further characterization.


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