BAX antibody (BCL2-Associated X Protein) (AA 43-61)

Details for Product anti-BAX Antibody No. ABIN967400, Supplier: Log in to see
Antigen
  • bax
  • fj16e01
  • wu:fc50b10
  • wu:fj16e01
  • bax-A
  • xBax
  • xlbax
  • BAX
  • BCL2L4
  • BAX-ALPHA
  • bcl2-associated X protein, a
  • BCL2-associated X protein
  • Bcl2-associated X protein
  • baxa
  • bax
  • BAX
  • Bax
  • LOC100355675
Alternatives
anti-Human BAX antibody for Immunohistochemistry (Paraffin-embedded Sections)
Epitope
AA 43-61
107
65
31
23
21
20
15
15
13
11
11
10
10
9
8
8
5
5
3
3
3
2
2
2
2
2
2
2
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Reactivity
Human
497
221
202
89
47
35
30
28
22
9
8
8
5
3
3
2
1
1
1
1
Host
Rabbit
322
204
4
Clonality
Polyclonal
Conjugate
This BAX antibody is un-conjugated
19
14
13
11
8
7
7
6
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
3
2
2
1
Application
Immunohistochemistry (Formalin-fixed Sections) (IHC (f)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunoprecipitation (IP), Western Blotting (WB)
383
208
144
135
121
116
97
48
40
35
13
9
5
5
4
2
1
1
1
1
1
Options
Supplier
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Supplier Product No.
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Brand BD Pharmingen™
Immunogen Human Bax aa. 43-61 synthetic peptide
Isotype Ig Fraction
Characteristics 1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
2. Please refer to us for technical protocols.
3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
4. This product contains thimerosal, an organic mercury compound. Mercury and mercury compounds are chemicals known to the State of California to cause birth defects or other reproductive harm. Foreseeable use of this product does not pose a known reproductive toxicity threat.
Purification The polyclonal antibody was purified from antiserum by negative adsorption and affinity chromatography.
Alternative Name Bax (BAX Antibody Abstract)
Background Bcl-2 family members are involved in mediating programmed cell death or apoptosis, and share two highly conserved functional regions, Bcl-2 homology 1 and 2 (BH1 and BH2). Several of the family members including Bcl-2 act as inhibitors of apoptosis, whereas others such as Bax promote cell death. It is thought that protein-protein interactions between Bcl-2 family members play an important role in their function. For example, Bax can homodimerize as well as heterodimerize with Bcl-2. When Bax is present in excess, it can counteract the ability of Bcl-2 to inhibit cell death. mRNA and protein studies indicate that Bax is more widely expressed than Bcl-2, suggesting that Bax has other functions besides inhibiting Bcl-2. For example, Bax has been shown to be directly induced by the tumor suppressor p53 in radiation sensitive cells, and thus may play a role in the apoptotic elimination of cells after their exposure to DNA-damaging agents. The Bax gene potentially encodes three different proteins Bax-alpha (21 kD), Bax-beta (24 kD) and Bax-gamma (5 kD). Bax-alpha is the most common transcript. The antibodies recognize human Bax. They do not cross-react with mouse Bax. A synthetic peptide corresponding to amino acids 43-61 of human Bax was used as immunogen. The specificity of the antiserum was verified by immunoprecipitation, western blot analyisis, and immunohistochemisty, as well as by comparisons with preimmune serum and by competition experiments.
Molecular Weight 21-22 kDa
Research Area Cancer, Apoptosis/Necrosis
Pathways p53 Signaling, PI3K-Akt Signaling, Apoptosis, Caspase Cascade in Apoptosis, Positive Regulation of Endopeptidase Activity, Unfolded protein response
Application Notes Applications include immunoprecipitation (1 µl/one million cells), western blot analysis (1:1000), and immunohistochemistry (1:1000) of acetone-fixed, frozen tissue sections and of formalin-fixed, paraffin-embedded tissue sections. Normal breast epithelium is suggested as a positive control for immunohistochemistry. MCF-7 human breast carcinoma cells (ATCC HTB-22) are suggested as positive controls for immunoprecipitation and western blot analysis. In western blots the antiserum detects Bax as a single band, thought to be Bax-alpha, of 21-22 kD in cell lines tested. The antiserum may also recognize Bax-beta.
Comment

Related Products: ABIN967390, ABIN968585

Restrictions For Research Use only
Format Liquid
Buffer Aqueous buffered solution containing ≤0.09 % sodium azide and ≤0.03 % thimerosal
Preservative Sodium azide, Thimerosal (Merthiolate)
Precaution of Use This product contains Sodium azide and Thimerosal (Merthiolate): POISONOUS AND HAZARDOUS SUBSTANCES which should be handled by trained staff only.
Storage 4 °C
Storage Comment Store undiluted at 4°C.
Product cited in: Ohta, Iwai, Kasahara, Taniguchi, Krajewski, Reed, Miyawaki: "Immunoblot analysis of cellular expression of Bcl-2 family proteins, Bcl-2, Bax, Bcl-X and Mcl-1, in human peripheral blood and lymphoid tissues." in: International immunology, Vol. 7, Issue 11, pp. 1817-25, 1996 (PubMed).

Krajewski, Krajewska, Shabaik, Miyashita, Wang, Reed: "Immunohistochemical determination of in vivo distribution of Bax, a dominant inhibitor of Bcl-2." in: The American journal of pathology, Vol. 145, Issue 6, pp. 1323-36, 1995 (PubMed).

Reed: "Bcl-2 and the regulation of programmed cell death." in: The Journal of cell biology, Vol. 124, Issue 1-2, pp. 1-6, 1994 (PubMed).

Yin, Oltvai, Korsmeyer: "BH1 and BH2 domains of Bcl-2 are required for inhibition of apoptosis and heterodimerization with Bax." in: Nature, Vol. 369, Issue 6478, pp. 321-3, 1994 (PubMed).

Oltvai, Milliman, Korsmeyer: "Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death." in: Cell, Vol. 74, Issue 4, pp. 609-19, 1993 (PubMed).

Background publications Krajewski, Blomqvist, Franssila, Krajewska, Wasenius, Niskanen, Nordling, Reed: "Reduced expression of proapoptotic gene BAX is associated with poor response rates to combination chemotherapy and shorter survival in women with metastatic breast adenocarcinoma." in: Cancer research, Vol. 55, Issue 19, pp. 4471-8, 1995 (PubMed).

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